Interest of Behavioural Reeducation in Dysfunctions of Masticatory Apparatus. Relations Between Parafunctions and Dysfunctions of Mastixatory Apparatus

NCT ID: NCT01535378

Last Updated: 2014-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

32 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-03-31

Brief Summary

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If etiologies of temporomandibular disorders (TMD) are various, parafunctions become more and more important. Treatment of patients presenting TMD is based on conservative and reversible therapeutics. The behavioural reeducation of these patients which aims at decreasing their parafunctions is a treatment often performed.

Detailed Description

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Conditions

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Temporomandibular Disorders

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Male and female over 18,
* Patient who was informed about the protocol and who did not refuse to take part in the programme,
* Patient who suffers of dysfunctions of masticatory apparatus: myofascial pain, joint clicking or crepitations, disc deplacement with reduction, mandibular limitation and/or deviation,
* Patient who presents more or less obvious parafunctions, which are associated or not to other etiologies
* Patient consulting for the 1st time for TMD

Exclusion Criteria

* Persons over 18 who are under legal protection (guardianship), persons who are deprived of their freedom,
* Patient who is already followed in the consultation of dysfunctions of masticatory apparatus and who is under treatment,
* Patient who is under treatment of occlusal splint (not in the framework of the consultation of TMD
* Patient with pains other than orofacial pains (cephalalgia, neuralgia, vascular algia of the face, migraine),
* Patient who needs a treatment other than a behavioural reeducation (pharmacological treatment, occlusal splint , addressed to another therapist, prosthetic treatment)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rennes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dominique Chauvel-Lebret

Role: PRINCIPAL_INVESTIGATOR

Rennes University Hospital

Locations

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Rennes University Hospital

Rennes, Brittany Region, France

Site Status

Countries

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France

Other Identifiers

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LOC/11-06

Identifier Type: OTHER

Identifier Source: secondary_id

2011-A00838-33

Identifier Type: -

Identifier Source: org_study_id

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