- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01679821
Prevalence of Signs and Symptoms of TMD in Patients Wearing Double Complete Dentures, RPD and in Dentistry Students.
September 5, 2012 updated by: Maristela Maria Galina Pezzini, Universidade Estadual do Oeste do Paraná
Prevalence of Signs and Symptoms of Temporomandibular Disorders (TMD) in Patients Wearing Double Complete Dentures, Removable Partial Dentures and Dentistry Students at State University of West of Paraná - UNIOESTE
It was proposed in this study to evaluate the prevalence of TMD signs and symptoms in State University of West of Parana's dental students with natural dentition, in patients with removable partial dentures and double complete dentures.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The Temporomandibular Disorder (TMD) has a high prevalence among the population.
Objectives: To evaluate the prevalence of signs and symptoms of TMD.
Methodology: 210 randomly selected individuals were evaluated, being divided into three groups with seventy individuals each: Group 1 - dental students with natural dentition.
Group 2 - patients with removable partial dentures.
And Group 3 - patients with double complete dentures.
The questionnaire of the American Academy of Orofacial Pain for triage was employed, then, clinical evaluation was carried out.
Study Type
Observational
Enrollment (Actual)
210
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Paraná
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Cascavel, Paraná, Brazil, 85819110
- Universidade Estadual do Oeste do Paraná
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Seventy dental students of State University of West of Paraná - UNIOESTE, seventy patients treated at the UNIOESTE Dental Clinic that wore removable partial denture (partially edentulous) and seventy patients with double complete dentures treated in Center for Dental Specialties of Cascavel, Paraná, Brazil.
Description
Inclusion Criteria:
- Patients wearing double complete denture, patients wearing just removable partial denture and dentate students.
Exclusion Criteria:
Students in orthodontic treatment or with less than one year after the end of orthodontic treatment were excluded from the research.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Dental students
Seventy dental students of State University of West of Paraná - UNIOESTE.
Students in orthodontic treatment or with less than one year after the end of orthodontic treatment were excluded from the research.
A questionnaire and a clinical examination were employed.
|
Seventy dental students of State University of West of Paraná - UNIOESTE, seventy patients treated at the UNIOESTE Dental Clinic that wore removable partial denture (partially edentulous) and seventy patients with double complete dentures treated in Center for Dental Specialties of Cascavel, Paraná, Brazil.
Students in orthodontic treatment or with less than one year after the end of orthodontic treatment were excluded from the research.
Patients wearing a complete denture in one maxillary and a removable partial denture in another maxillary, and patients wearing just one complete denture were not included in the research.
|
Removable partial denture
Seventy patients treated at the UNIOESTE Dental Clinic that wore removable partial denture (partially edentulous).
Patients wearing a complete denture in one maxillary and a removable partial denture in another maxillary were not included in the research.
A questionnaire and a clinical examination were employed.
|
Seventy dental students of State University of West of Paraná - UNIOESTE, seventy patients treated at the UNIOESTE Dental Clinic that wore removable partial denture (partially edentulous) and seventy patients with double complete dentures treated in Center for Dental Specialties of Cascavel, Paraná, Brazil.
Students in orthodontic treatment or with less than one year after the end of orthodontic treatment were excluded from the research.
Patients wearing a complete denture in one maxillary and a removable partial denture in another maxillary, and patients wearing just one complete denture were not included in the research.
|
Double complete denture
Seventy patients with double complete dentures treated in Center for Dental Specialties of Cascavel, Paraná, Brazil.
Patients wearing just one complete denture were not included in the research.
A questionnaire and a clinical examination were employed.
|
Seventy dental students of State University of West of Paraná - UNIOESTE, seventy patients treated at the UNIOESTE Dental Clinic that wore removable partial denture (partially edentulous) and seventy patients with double complete dentures treated in Center for Dental Specialties of Cascavel, Paraná, Brazil.
Students in orthodontic treatment or with less than one year after the end of orthodontic treatment were excluded from the research.
Patients wearing a complete denture in one maxillary and a removable partial denture in another maxillary, and patients wearing just one complete denture were not included in the research.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Assessment of the prevalence of signs and symptoms of temporomandibular disorders in patients with removable partial dentures, complete double dentures and toothed.
Time Frame: 5 months
|
5 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
questionnaire for selection of orofacial pain and temporomandibular disorders recommended by the American Academy of Orofacial Pain
Time Frame: 5 monts
|
5 monts
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clinical examination
Time Frame: 5 months
|
A clinical examination, which was divided into parts, namely: identification and analysis; part of the Axis I of RDC/TMD - Research Criteria for Temporomandibular Disorders; muscle palpation; and for patients with dentures, the history and clinical evaluation of them
|
5 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Maristela Pezzini, Professor, Universidade Estadual do Oeste do Paraná
- Principal Investigator: Thaisa Bordin, Student, Universidade Estadual do Oeste do Paraná
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2010
Primary Completion (Actual)
March 1, 2011
Study Completion (Actual)
August 1, 2011
Study Registration Dates
First Submitted
September 1, 2012
First Submitted That Met QC Criteria
September 5, 2012
First Posted (Estimate)
September 6, 2012
Study Record Updates
Last Update Posted (Estimate)
September 6, 2012
Last Update Submitted That Met QC Criteria
September 5, 2012
Last Verified
September 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 538/2010-CEP
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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