- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01679821
Prevalence of Signs and Symptoms of TMD in Patients Wearing Double Complete Dentures, RPD and in Dentistry Students.
5. september 2012 opdateret af: 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.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
210
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Paraná
-
Cascavel, Paraná, Brasilien, 85819110
- Universidade Estadual do Oeste do Paraná
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
19 år til 90 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Sandsynlighedsprøve
Studiebefolkning
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.
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
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.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Assessment of the prevalence of signs and symptoms of temporomandibular disorders in patients with removable partial dentures, complete double dentures and toothed.
Tidsramme: 5 months
|
5 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
questionnaire for selection of orofacial pain and temporomandibular disorders recommended by the American Academy of Orofacial Pain
Tidsramme: 5 monts
|
5 monts
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Clinical examination
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Maristela Pezzini, Professor, Universidade Estadual do Oeste do Paraná
- Ledende efterforsker: Thaisa Bordin, Student, Universidade Estadual do Oeste do Paraná
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. december 2010
Primær færdiggørelse (Faktiske)
1. marts 2011
Studieafslutning (Faktiske)
1. august 2011
Datoer for studieregistrering
Først indsendt
1. september 2012
Først indsendt, der opfyldte QC-kriterier
5. september 2012
Først opslået (Skøn)
6. september 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
6. september 2012
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
5. september 2012
Sidst verificeret
1. september 2012
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 538/2010-CEP
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .