- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01679821
Prevalence of Signs and Symptoms of TMD in Patients Wearing Double Complete Dentures, RPD and in Dentistry Students.
5. September 2012 aktualisiert von: 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.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Beobachtungs
Einschreibung (Tatsächlich)
210
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Paraná
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Cascavel, Paraná, Brasilien, 85819110
- Universidade Estadual do Oeste do Paraná
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
19 Jahre bis 90 Jahre (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Ja
Studienberechtigte Geschlechter
Alle
Probenahmeverfahren
Wahrscheinlichkeitsstichprobe
Studienpopulation
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.
Beschreibung
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.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
Kohorten und Interventionen
Gruppe / Kohorte |
Intervention / Behandlung |
|---|---|
|
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.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Assessment of the prevalence of signs and symptoms of temporomandibular disorders in patients with removable partial dentures, complete double dentures and toothed.
Zeitfenster: 5 months
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5 months
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
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questionnaire for selection of orofacial pain and temporomandibular disorders recommended by the American Academy of Orofacial Pain
Zeitfenster: 5 monts
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5 monts
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Clinical examination
Zeitfenster: 5 months
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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
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5 months
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Ermittler
- Hauptermittler: Maristela Pezzini, Professor, Universidade Estadual do Oeste do Paraná
- Hauptermittler: Thaisa Bordin, Student, Universidade Estadual do Oeste do Paraná
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. Dezember 2010
Primärer Abschluss (Tatsächlich)
1. März 2011
Studienabschluss (Tatsächlich)
1. August 2011
Studienanmeldedaten
Zuerst eingereicht
1. September 2012
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
5. September 2012
Zuerst gepostet (Schätzen)
6. September 2012
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
6. September 2012
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
5. September 2012
Zuletzt verifiziert
1. September 2012
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 538/2010-CEP
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