Skip to main content
Clinical Trials/NCT04951895
NCT04951895
Completed
Not Applicable

Clinical and MRI Finding of The Temporomandibular Joint Posterior Disk Displacement

Al-Azhar University1 site in 1 country900 target enrollmentFebruary 20, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
TMJ Disc Disorder
Sponsor
Al-Azhar University
Enrollment
900
Locations
1
Primary Endpoint
VAS
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

the study aimed to evaluate the clinical and MRI finding of TMJ with posterior disk displacement with predication of the risk factors

Detailed Description

: the study aimed to evaluate the clinical and MRI finding of TMJ with posterior disk displacement with predication of the risk factors. Study design: this retrospective study included patients diagnosed as TMJ internal derangement and all the patients examined by MRI from 2008 to 2019. Cases with loss of continuity of articular disk or the posterior attachment of the disk were considered as positive cases.

Registry
clinicaltrials.gov
Start Date
February 20, 2020
End Date
June 15, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ayman Hegab

associate professor of oral and maxillofacial surgery

Al-Azhar University

Eligibility Criteria

Inclusion Criteria

  • patients seeking treatment for TMD at Al-Azhar University Hospital and the outpatient clinic at the Faculty of Dental Medicine of Al-Azahr University

Exclusion Criteria

  • Patients were included if they were older than 18 years and diagnosed with TMJD. criteria for this study included systemic diseases (the presence of polyarthritis or other rheumatic diseases), contraindications for MRI (e.g., implanted metal or medical devices, claustrophobia), the presence of neurologic disorders, head and neck cancer, oral submucous fibrosis, a history of TMJ surgery, a history of previous nonsurgical treatment such as occlusal splints, and a history of joint injection with HA/PRP. Trauma patients with subcondylar fracture and patients with congenital and developmental disorders of the TMJ were also excluded from the study.

Outcomes

Primary Outcomes

VAS

Time Frame: baseline (pre treatment)

posttreatment pain index scores were measured using a 10-point visual analogue scale (VAS), with 0 indicating absence of pain and 10 indicating the worst pain.

mouth opening

Time Frame: baseline (pre treatment)

maximum nonassisted (voluntary) mouth opening (MVMO) in millimetres

Secondary Outcomes

  • joint sound(baseline (pre treatment))

Study Sites (1)

Loading locations...

Similar Trials