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NCT06013059 Clinical Trial

A Comparative Study Between the Different Levels of TMJ Arthroscopy in the Management of TMJ Internal Derangement

TMJ Disc Disorder Clinical Trial

Official title:
A Comparative Study Between the Different Levels of TMJ Arthroscopy in the Management of TMJ Internal Derangement (A Randomized Clinical Trial)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06013059
Other study ID # 001056 - IORG 0008839
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2021
Est. completion date July 30, 2023

Study information
Verified date October 2023
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The temporomandibular joint (TMJ) arthroscopy has emerging role nowadays in the treatment of TMJ internal derangement with its three levels of intervention. A comparative study between the 3 levels is essential to develop a standardized selection criteria and management algorithm.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date July 30, 2023
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients with TMJ internal derangement Wilkes III Exclusion Criteria: 1. Medically unfit patients. 2. Patients with TMDs secondary to malocclusion. 3. Psychological instability. 4. Patients operated before for other TMJ problems.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• three levels of TMJ arthroscopy
Group I: 10 patients will be treated with Lysis and lavage
• three levels of TMJ arthroscopy
Group II: 10 patients will be treated with operative arthroscopy
• three levels of TMJ arthroscopy
Group III: 10 patients will be treated with operative arthroscopy + discopexy

Locations
Country Name City State
Egypt Alexandria University Alexandria

Sponsors (1)
Lead Sponsor Collaborator
Alexandria University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mouth opening measurement measuring the maximal interincisal opening (MIO) 1, 3 and 6 months postoperatively
See also
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Recruiting NCT05983653 - Evaluation of Arthrocentesis With and Without PRP Injection in Patients With Disc Displacement With Reduction. N/A
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