UNIVERSIDADE ESTADUAL PAULISTA
JÚLIO DE MESQUITA FILHO”
Instituto de Ciência e Tecnologia
Campus de São José dos Campos
ORIGINAL ARTICLE DOI: https://doi.org/10.4322/bds.2024.e4353
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Braz Dent Sci 2024 July/Sept;27 (3): e4353
This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in
any medium, provided the original work is properly cited.
A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
Ensaio clínico randomizado de uma técnica simplificada para confecção de próteses totais: percepções do paciente,
eficiência mastigatória, disfunções temporomandibulares e qualidade das próteses
Ana Luísa Barros PASCOAL1 , Marcília Ribeiro PAULINO2 , Angelo Giuseppe Roncalli da Costa OLIVEIRA1 ,
Adriana da Fonte Porto CARREIRO1 , Wilson MESTRINER JÚNIOR3 , Patrícia dos Santos CALDERON1
1 - Universidade Federal do Rio Grande do Norte, Departamento de Odontologia. Natal, RN, Brazil.
2 - Universidade Federal de Pernambuco, Departamento de Odontologia. Recife, PE, Brazil.
3 - Universidade de São Paulo, Faculdade de Odontologia de Ribeirão Preto. Ribeirão Preto, SP, Brazil.
How to cite: Pascoal ALB, Paulino MR, Oliveira AGRC, Carreiro AFP, Mestriner Júnior W, Calderon PS. A randomized clinical trial of
a simplied technique for complete denture fabrication: patient perceptions, masticatory efciency, temporomandibular disorders and
quality of dentures. Braz Dent Sci. 2024;27(3):e4353. https://doi.org/10.4322/bds.2024.e4353
ABSTRACT
Objective: To evaluate the efcacy of a simplied technique for complete dentures (CD) fabrication focusing
on patient-reported outcome measures (PROMs), masticatory efciency (ME), temporomandibular disorders
(TMD), and CD technical quality. Material and Methods: Fifty edentulous individuals were allocated into two
groups based on the complete denture (CD) fabrication method: traditional (T) or simplied (S). Patients were
evaluated at baseline and at a 3-month follow-up, considering quality of life and satisfaction. The technical quality
of the CDs and masticatory efciency were assessed at the 3-month follow-up using a validated instrument and
a colorimetric test, respectively. Data were analyzed using McNemar and Mann-Whitney tests for intra-group
comparisons and Chi-square, Fisher’s Exact, or Wilcoxon tests for inter-group comparisons. Results: Forty-two
patients completed the study (T = 20, S = 22). At the 3-month follow-up, no signicant differences were observed
between the groups for masticatory efciency (p = 0.131), CD technical quality (p = 0.456), satisfaction (p =
0.146), and quality of life (p = 0.409). Patient-reported outcome measures (PROMs) improved from baseline
to the 3-month follow-up (p < 0.01) for both groups. The presence of temporomandibular disorders (TMD)
signicantly decreased after denture replacement (p < 0.001). Conclusion: CD fabricated by a simplied
technique seems to be time-efcient and as effective as that fabricated by a traditional technique. Insertion of
new dentures positively inuenced PROMs and TMD presence.
KEYWORDS
Complete denture; Mastication; Patient satisfaction; Quality of life; Temporomandibular disorders.
RESUMO
Objetivo: Avaliar a ecácia de uma técnica simplicada para fabricação de próteses totais (PT) nos desfechos
relatados pelo paciente (PROMs), eciência mastigatória (EM), difunções temporomandibulares (DTM) e qualidade
técnica da prótese. Material e Métodos: 50 indivíduos edêntulos foram alocados em dois grupos com base no
método de fabricação da prótese total (PT): tradicional (T) ou simplicado (S). Os pacientes foram avaliados
antes e 3 meses após a instalação das próteses, considerando a qualidade de vida e a satisfação. A qualidade
técnica das PTs e a eciência mastigatória foram avaliadas no seguimento de 3 meses usando um instrumento
validado e um teste colorimétrico, respectivamente. Os dados foram analisados usando os testes de McNemar
e Mann-Whitney para comparações intra-grupo e os testes Qui-quadrado, Exato de Fisher ou Wilcoxon para
comparações entre os grupos. Resultados: Quarenta e dois pacientes completaram o estudo (T = 20, S = 22).
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Braz Dent Sci 2024 July/Sept;27 (3): e4353
Pascoal ALB et al.
A randomized clinical trial of a simplified technique for complete denture fabrication: patient perceptions, masticatory efficiency, temporomandibular disorders and quality of dentures
Pascoal ALB et al. A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
INTRODUCTION
Edentulism, the condition characterized
by the loss of all natural teeth, has signicant
implications for oral health and overall well-
being. It is a devastating and irreversible condition
and one of the public health burdens for elderly
people and effects clearly the practice of primary
care [1]. Factors contributing to edentulism
include age, socioeconomic status, and access
to dental care [2]. There is a notable decline in
edentulism in recent years, marking a positive
shift in oral health trends worldwide. However,
the edentulism is still prevalent and can continue
to increase until 2040 [3]. This trend reects
the historical focus of public oral health care for
adults on urgent care, which often involves tooth
extractions [3,4].
To reduce clinical and laboratory steps
during denture fabrication, simplied techniques
for complete denture (CD) fabrication have been
developed. These approaches appear to be as
effective as traditional approaches while requiring
less time and resources [5]. There is no evidence
that dentures made using traditional techniques
are preferred by patients over those made using
simplied techniques [6]. The complete dentures
must also provide retention and stability, which
may be affected by the manufacturing process [7].
Masticatory ability can also be influenced by
technical quality [5]. The degree of residual ridge
atrophy and the duration of edentulism may also
have an impact on treatment success and may
introduce bias when comparing CD fabrication
techniques [8-10].
Several variables, including those assessed
by professionals and patient-reported outcome
measures (PROMs) [11], must be investigated
to assess the effectiveness of simplied methods.
Patient satisfaction should be taken into account
during rehabilitation treatment, especially since
it is associated to patients’ adaptation, as well as
comfort, aesthetics, chewing, and phonetics [6].
The assessment of Oral Health-Related Quality
of Life (OHRQoL) has been considered essential
in determining an individual’s quality of
life [12], as oral rehabilitation encompasses
psychological and social aspects in addition to
physical health [12]. A widely used instrument
for assessing OHRQoL in edentulous patients
is the OHIP-EDENT [13]. This inventory has
demonstrated strong psychometric properties,
enabling the evaluation of the impact of oral
rehabilitation on both the functional aspects and
quality of life of edentulous individuals [14].
Epidemiological studies have reported the
presence of Temporomandibular Disorders (TMD)
in complete dentures (CD) patients; however,
there is no consensus regarding the prevalence
of these disorders in these patients [5,15]. Most
CD wearers are elderly and the prevalence of
TMD in this population is controversial. Authors
such as Schmitter et al. [16] claim that elderly
patients may exhibit signs and symptoms of TMD,
but rarely complain of pain. Literature is still
controversial regarding the factors that contribute
to the development of TMD in CD wearers [6].
For instance, Sanjeevan et al. [17] in a meta-
analysis, compare simplied and traditional CD
production techniques and found no differences
in patient satisfaction or technical quality.
The authors also observed that the simplied
technique made less expensive and time efcient
CD. However, while some studies support the
efficacy of simplified techniques, the limited
number of randomized clinical trials using
similar clinical methodologies and differences
in simplied techniques in the literature did not
support the use of such a technique.
Simplied techniques for CD offer signicant
benefits in terms of cost, time efficiency, and
3 meses após a instalação das PTs não foram observadas diferenças signicativas entre os grupos quanto à
eciência mastigatória (p = 0,131), qualidade técnica das PTs (p = 0,456), satisfação (p = 0,146) e qualidade
de vida (p = 0,409). Os desfechos relatados pelos pacientes (PROMs) melhoraram 3 meses após a instalação
das próteses (p < 0,01) para ambos os grupos. A presença de disfunções temporomandibulares (DTM) diminuiu
signicativamente após a substituição das próteses (p < 0,001). Conclusão: As PTs fabricadas pela técnica
simplicada parecem ser tão ecazes quanto aquelas fabricadas pela técnica tradicional. A inserção de novas
PTs inuenciou positivamente os PROMs e a presença de DTM.
PALAVRAS-CHAVE
Prótese total; Mastigação; Satisfação do paciente; Qualidade de vida; Disfunções temporomandibulares.
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Braz Dent Sci 2024 July/Sept;27 (3): e4353
Pascoal ALB et al.
A randomized clinical trial of a simplified technique for complete denture fabrication: patient perceptions, masticatory efficiency, temporomandibular disorders and quality of dentures
Pascoal ALB et al. A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
accessibility. However, they also present trade-offs,
particularly concerning customization for patients
with anatomical limitations, overall quality, and
improvements in PROMs. The propose of this
research is evaluate the efficacy of a simplified
CD fabrication technique in terms of PROMs,
masticatory efficiency, TMD, and CD technical
quality. Given that this is an equivalence trial, our
expectation was that the simplied technique would
demonstrate efficacy comparable to traditional
methods while being more cost-effective and time-
efcient. The null hypothesis was that there is no
difference between the S and T techniques with
respect to the parameters analyzed.
MATERIAL AND METHODS
This randomized clinical trial was entered
into the clinicaltrials database (identifier:
NCT02652403). Each patient provided written
informed consent in accordance with the
regulations of the local Research Ethics Committee
(protocol number: 37098714.5.0000.5292).
The sample size calculation was according to
prior study Regis et al. [6]. The power test was
calculated using Sealed Envelop Ltd software
(https://www.sealedenvelope.com/power/
continuous-equivalence/) at 80% and the 95%
condence interval and considering a standard
deviation of 2.99 from General Ohip-Edent [6]
with a minimum sample of 18 patients per group,
anticipating possible sample loss, 25 patients’
group were adopted.
The sole inclusion criterion was the use
of previous dentures (in both jaws) for at least
one year, while the exclusion criterion was the
presence of pathological changes in the alveolar
ridges (such as CD-induced brous hyperplasia).
A standardized preliminary alginate impression
using edentulous metal tray was made for all
patients. Subsequently, patients were randomly
assigned, using a sealed envelope, to one of two
groups: traditional technique, considered the
control group (T), or simplied technique (S).
Patients were blinded to their assigned study
group.
The treatment was carried out by four
experienced prosthodontists in accordance with
a standardized clinical protocol. The clinical
protocol for the traditional technique was
similar to previous studies [5,6,12] and the
simplied technique consisted of four chair-side
and three laboratory steps (as detailed in the
Table I). The initial alginate impression was
standardized and consistent across groups, and
it was made with metal-perforated edentulous
impression trays that were wax-lined on the
border using soft utility wax (to minimize border
over extension). The work casts based on the
alginate impression and the arbitrary mount on
SAA (using a 15 degrees plan) in the S group
were the differences between the traditional and
simplied methods [6].
The post dam was created arbitrarily, by
marking the work cast, for the S group and during
Table I - Chair-side and laboratory steps of the two methods
Step Traditional Simplified
1 Chair-side Preliminary alginate impression
(edentulous metal trays) Final alginate impression (edentulous metal trays)
2 Laboratory Primary casts and custom trays fabrication
(auto polymerizing acrylic) Work casts and occlusal rims fabrication
3 Chair-side Secondary impression (impression compounds and
Zinc oxide–eugenol paste)
Jaw registration (vertical dimension and centric
relation), teeth shade selection and casts arbitrarily
mount on SAA (using a 15 degrees plan)
4 Laboratory Work casts and occlusal rims fabrication Teeth set-up (33-degree teeth and mutually protected
occlusion)
5 Chair-side
Jaw registration (vertical dimension and centric
relation), teeth shade selection and casts mount on
SAA using face-bow
Teeth try-in
6 Laboratory Teeth set-up (33-degree teeth and mutually protected
occlusion) Laboratorial finishing process
7 Chair-side Teeth try-in Denture insertion
8 Laboratory Laboratorial finishing process
9 Chair-side Denture insertion
SAA: semi adjustable articulator.
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Braz Dent Sci 2024 July/Sept;27 (3): e4353
Pascoal ALB et al.
A randomized clinical trial of a simplified technique for complete denture fabrication: patient perceptions, masticatory efficiency, temporomandibular disorders and quality of dentures
Pascoal ALB et al. A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
the custom tray adjustment, before the secondary
impression, for the T group. The denture insertion
appointment was conducted similarly for both
groups. Before insertion, professionals checked
the surface polish and border design of the
dentures. After inserting the CDs, they assessed
border extension and fit, retention, stability,
and occlusal contacts. If the patient reported
any discomfort or if any occlusal disharmony
was observed, the professional performed the
necessary adjustments followed by a polishing
procedure.
Patients completed a general information
inventory at the baseline (gender, age, and years
of use of the previous CD). A calibrated examiner
performed a clinical evaluation of mandibular
residual ridge height, which was classified
according to prognosis: high and medium (better
prognosis), or low residual ridge height (worst
prognosis). The follow-up appointments were
scheduled for 24 hours, 7, 14, and 30 days,
and 3 months after the CD insertion. However,
additional follow-up appointments could be
scheduled if necessary, for instance, if the patient
had any complaints.
PROMs and TMD presence were assessed
at baseline, while patients wore their previous
CD. PROMs were evaluated by a satisfaction
inventory [6] and using the Portuguese version
of OHIP-Edent [13]. Ohip-Edent questions were
grouped into subclasses [6,18]. All subclasses
were comprised of 5 questions, with scores
ranging from 0 to 10 points, except for the
psychological discomfort and disability subclasses,
with 4 four questions and scores ranging from
0 to 8 points. The presence of TMD was assessed
by the Portuguese version of RDC/TMD [19]
and all TMD patients were classied based on
TMD origin (myogenous or arthrogenous or
myogenous and arthrogenous).
Masticatory efciency was assessed using
mastication capsules in combination with a
colorimetric method, as described previously
by Santos et al. [20]. All patients were properly
seated in chairs and instructed to chew the capsule
for 20 seconds. A spectrophotometer (Ultrospec
2100 pro UV / Visible Spectrophotometer, GE
Healthcare, New York, USA) was used to measure
the concentration of the staining intensity of
the fuchsin solution, which was expressed as
absorbance (abs).
The CD quality was assessed using the
Sato et al. [7] instrument, which evaluates:
anterior teeth arrangement, interocclusal
distance, stability of mandibular denture,
occlusion, articulation, retention of mandibular
denture, and border extension of mandibular
denture. Each item was assigned a conversion
number (0-18) based on the scores assigned
(1-3). The general quality of the prosthesis score
ranges from 0 to 100, and 100 indicate better
quality and 0, poor quality.
Examiners calibrated and blinded for
patients group collected data. The same examiner
assessed PROMs and the presence of TMD at
baseline and three months later. Masticatory
efciency and CD quality were only assessed after
a three-month follow-up, to assess patients after
the adaptation period.
Statistical analysis
SPSS software (Statistical Package for Social
Sciences) for Windows, version 20.0, was used to
analyze the data. Baseline data were compared
using the Mann-Whitney, Pearson’s chi-square
or Fisher’s exact tests. The TMD diagnosis was
compared before and after the CD insertion
using the Pearson Chi-square test. The TMD
origin was evaluated using the Mann-Whitney,
Pearson’s Chi-square, and Fisher’s Exact tests.
The satisfaction analysis used the Chi-square test,
Fisher’s Exact test (for inter-group comparison),
and the McNemar test (for intra-group ratings).
For OHIP analysis, the Mann-Whitney test (for
inter-group comparison) and the Wilcoxon
test (for intra-group evaluations) were used.
The Mann-Whitney test was used to evaluate
masticatory efciency and denture quality. A 5%
signicance level was used.
RESULTS
Fifty patients were selected and randomly
assigned to one of two groups: T (N=25) or
S (N=25). There were 44 females (88%) and
6 males (12%). The participants’ ages ranged
from 50 to 92 years, and their previous CD
use ranged from 1 to 30 years. At the baseline,
there were no statistical differences between
the groups (Table II). At the 3-month follow-up,
8 participants dropped out of the study for various
reasons (Figure 1). As a result, the nal sample
included 42 patients (38 females and 4 males)
with an average age of 65.96 ± 9.35 years.
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Braz Dent Sci 2024 July/Sept;27 (3): e4353
Pascoal ALB et al.
A randomized clinical trial of a simplified technique for complete denture fabrication: patient perceptions, masticatory efficiency, temporomandibular disorders and quality of dentures
Pascoal ALB et al. A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
The level of adjustment required for the CD
at the insertion appointment was similar for both
groups. On average, patients in the S group needed
2.4 additional follow-up appointments, while
patients in the T group needed 2.9 (p = 0.568).
PROMs evaluation revealed no statistically
signicant differences between groups at baseline
(p=0.662) and 3-month follow-up for or general
OHIP-Endent (p=0.409). Same result was
observed in for general satisfaction baseline
(p=0.381) and 3-month follow-up (p=0.146).
The intragroup (from baseline to 3-month follow
up) analysis revealed significant differences
in OHIP-Edent, p<0.01 for both groups and
in satisfaction for the majority of the assessed
aspects (p<0.05), but not for “pain-maxillary
arch,” (p= 0.500) “adaptation-maxillary arch,”
(p=0.500) and “retention maxillary arch”
(p=0.125) for the S group.
Table II - Baseline characteristics of the sample
Group
Overall
p
T S
Age (years) 64 (57.5-72) 65 (61.5-75) 65 (58.75-72) 0.225
Gender
-Female 22 (88%) 22 (88%) 44 (88%)
Male 3 (12%) 3 (12%) 6 (12%)
Use of previous CD (years)
Maxillary 6 (3-13.5) 9 (4.5-10) 8 (4-12) 0.430
Mandibular 7 (3-15) 8 (4-10) 8 (4-12) 0.992
Height of the mandibular residual ridge
High / medium 7 (28%) 6 (24%) 13 (26%) 0.500*
Low 18 (72%) 19 (76%) 37 (74%)
T: Traditional, S: Simplified. Median (interquartile range) for age, and previous use of last complete denture (CD). Other variables in absolute
values (%). Mann- Whitney test, Chi Square test*. (-) Tests not applicable. Significant difference, p<0.05.
Figure 1 - Study flow diagram.
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Braz Dent Sci 2024 July/Sept;27 (3): e4353
Pascoal ALB et al.
A randomized clinical trial of a simplified technique for complete denture fabrication: patient perceptions, masticatory efficiency, temporomandibular disorders and quality of dentures
Pascoal ALB et al. A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
At baseline, the RDC/TMD identified
28 (56%) TMD patients (myogenous = 1,
arthrogenous = 19, and myogenous and
arthrogenous = 8). At the 3-month follow-up,
23 TMD patients were evaluated, 11 (45.8%)
showed improvements (5 patients classied as
non-TMD and 6 improving from myogenous and
arthrogenous to myogenous or arthrogenous)
and 12 (54.2%) remaining stable. No patient
worsened, and all patients who did not have TMD
at baseline remained so at the 3-month follow-up.
At 3 months of follow-up, the inter-group analysis
of TMD diagnosis revealed no difference between
groups (p=0.530). For the entire sample, there
was a signicant difference (p=0.001) in the
presence of TMD before and after CD insertion.
The mean masticatory efficiency of the
patients was 0.055 ± 0.029 abs and the average
score for the CD quality for both groups was
83.19 ± 11.07, with no statistical differences
between groups (p>0.05). The entire sample
was then evaluated according to the fabrication
technique (T or S) and height of the mandibular
residual ridge (High / medium or low) with
regard to masticatory efciency and CD quality.
No difference was observed for masticatory
efficiency (p=0 >0.05) in both assessments.
For CD quality, regarding the fabrication
technique, there was no difference (p= 0.456),
however there was a significant statistical
difference in view of the height of the mandibular
residual ridge (p = 0.009), and the CD quality
was greater for high/medium edentulous ridges
(Table III).
DISCUSSION
The present randomized clinical trial evaluated
a simplied technique for complete denture (CD)
fabrication, focusing on patient-reported outcome
measures (PROMs), masticatory efciency (ME),
temporomandibular disorders (TMD), and CD
technical quality. The results indicated no signicant
differences between the fabrication techniques
concerning the analyzed variables, leading to the
acceptance of the null hypothesis. Additionally,
the study demonstrated that PROMs may improve
after suitable CD replacement, irrespective of
the fabrication technique. These findings are
consistent with previous studies by Kawai et al. [21],
Regis et al. [6], Komagamine et al. [12] and
Tôrres et al. [22].
Although the CD quality was not assessed
at the baseline, the authors believe that the
improvement in PROMs is attributed to the new
CD’s aesthetic and functional reestablishment.
The previous CD was used, by the majority of the
sample, for more than 5 years. This prolonged
use may result in poor adaptation, CD wear, and
changes in the vertical dimension, all of which are
known to have a negative impact on CD retention,
chewing, and phonetics, resulting in higher levels
of dissatisfaction [23] and reduced OHRQoL.
Despite the fact that the majority of the
patients were diagnosed with TMD at the
baseline, none of them had TMD as their primary
complaint. The presence of TMD was similar
in both groups at the 3-month follow-up, but
some individuals showed an improvement after
CD replacement. Abdelnabi et al. [24] and
Goiato et al. [25] found similar results. These
results may be related to the restoration of
vertical dimension and centric relation, yielding
mandibular and muscles stability and driving to
the decrease of TMD signs and symptoms [24,25].
Since the fabrication technique seems not
to inuence the masticatory efciency, variables
such as age, gender, duration of edentulism,
residual ridge, and previous experiences can
affect it [8]. Koshino et al. [8] found a signicant
correlation between the basal area of the
mandibular residual ridge with masticatory
ability. However, no statistical correlation was
Table III - Patients’ masticatory efficiency, in abs and complete denture quality
n Masticatory efficiency
p
CD quality
p
Technique
0.456Traditional 20 0.046 (0.031-0.056) 0.131 83 (77-96)
Simplified 22 0.056 (0.038-0.078) 84 (73.75-89.75)
Height of the mandibular residual ridge
0.009*High / medium 12 0.055 (0.032-0.079) 0.449 88.5 (81.5-95)
Low 30 0.049 (0.033-0.062) 80.5 (72.5-86)
Median (interquartile range). Sample size (n) in absolute values. Mann- Whitney test. Significant difference, p<0.05.
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Braz Dent Sci 2024 July/Sept;27 (3): e4353
Pascoal ALB et al.
A randomized clinical trial of a simplified technique for complete denture fabrication: patient perceptions, masticatory efficiency, temporomandibular disorders and quality of dentures
Pascoal ALB et al. A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
found between masticatory efciency and other
variables in our study. This could be explaining
by factors such as harmful previous experience
or patients’ expectations [9].
Border molding procedures are thought to
be necessary for adequate CD retention, stability,
and support [26] however, in our study, the
omission of this step did not impact the overall
quality of the CD or the retention and stability of
the mandibular CD. These ndings are supported
by the literature [6,21,27,28].
Reabsorbed ridges can have a detrimental
effect on the impression process [8] In our study,
the mandibular residual ridge’s reduced height
led to a signicant decrease in the quality of the
CD. Ribeiro et al. [10] found similar results to
ours when they investigated whether the shape of
the jaw was related to CD retention and stability.
Evaluating only patients with severely resorbed
mandible Albuquerque et al. [29,30] compare one-
vs two-step impression procedures for complete
denture fabrication and did not observe differences
between techniques in relation to PROMs, quality
of the prostheses and chewing. As such, careful
execution of preliminary impressions, taking into
account the anatomy of the residual ridge, seems
to produce CD with comparable technical quality
to the traditional technique.
A recent meta-analysis has observed that
complete dentures produced using the simplied
method exhibit significantly lower costs and
reduced manufacturing time compared to those
produced through traditional methods [17].
Consequently, the ndings from this clinical trial
are promising and hold particular signicance for
public health dental systems. The 2010 Brazilian
oral health survey (SBBrasil 2010) highlighted a
considerable demand for prosthetic rehabilitation,
particularly among the elderly population.
Despite this, the number of dentures fabricated
remains insufcient in meeting the treatment
needs of the population.
Studies using simplied complete denture
(CD) techniques involving digital dentures [31,32]
have demonstrated that CDs fabricated through
these methods are as effective as those produced
using traditional methods in terms of patient-
reported outcome measures (PROMs). Moreover,
digital dentures reduce production time and cost,
and provide a more efcient means of storing
and retrieving patient records. However, there
are disadvantages to this technology, including
the signicant investment required for equipment
and training, and potentially limited levels of
customization compared to traditional methods.
Reducing the number of visits to CD
fabrication results in a positive response of
patent’s satisfaction [33]. Employ a simplied
technique for fabricating complete dentures in
in specialized dental centers could enable the
rehabilitation of a greater number of patients
with more efficient utilization of financial
resources [34,35]. Moreover, streamlining
clinical sessions has the potential to enhance
patient adherence to treatment, particularly
among individuals with limited mobility [35,36].
The short follow-up period of our study should
be considered as a limitation. Future research
should focus on longer-term follow-up to conrm
our findings and also explore the integration
of advanced digital technologies in simplied
CD fabrication techniques to enhance clinical
outcomes and PROMs.
CONCLUSION
Within the limitations of this current study, it
was concluded that complete dentures fabricated
by a simplied technique seems to be time-efcient
and as effective as that fabricated by a traditional
technique. The insertion of new dentures positively
inuenced PROMs and TMD presence.
Author’s Contributions
ALBP: Investigation, Formal Analysis,
Writing – Original Draft Preparation. MRP:
Investigation, Formal Analysis, Writing
Original Draft Preparation. AGRCO: Supervision,
Formal Analysis. AFPC: Supervision, Funding
Acquisition. WMJ: Funding Acquisition. PSC:
Conceptualization, Writing Review & Editing,
Project Administration, Supervision, Funding
Acquisition.
Conict of Interest
No conicts of interest declared concerning
the publication of this article.
Funding
This study was financed in part by the
Coordenação de Aperfeiçoamento de Pessoal de
Nível Superior - Brasil (CAPES) - Finance Code 001.
8
Braz Dent Sci 2024 July/Sept;27 (3): e4353
Pascoal ALB et al.
A randomized clinical trial of a simplified technique for complete denture fabrication: patient perceptions, masticatory efficiency, temporomandibular disorders and quality of dentures
Pascoal ALB et al. A randomized clinical trial of a simplified technique for complete
denture fabrication: patient perceptions, masticatory efficiency,
temporomandibular disorders and quality of dentures
Regulatory Statement
This study was conducted in accordance with
all the provisions of the local human subjects
oversight committee guidelines and policies
of: Federal University of Rio Grande do Norte
Research Ethical Comitee.
The approval code for this study is:
7098714.5.0000.5292.
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Patrícia dos Santos Calderon
(Corresponding address)
Universidade Federal do Rio Grande do Norte, Departamento de Odontologia,
Natal, RN, Brazil.
Email: patriciascalderon@yahoo.com.br
Date submitted: 2024 Apr 25
Accept submission: 2024 Aug 06