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Completed

NCT Number: NCT04951895

Clinical and MRI Finding of The Temporomandibular Joint Posterior Disk Displacement

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

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Key information

Conditions

Age range

19 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Faculty of Dental Medicine Alazhar University

Cairo, Nasr City, 11765, Egypt

About this study

: 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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

MRI

Diagnostic Test

MRI of TMJ

Primary outcomes

  1. 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.

  2. mouth opening

    Time frame: baseline (pre treatment)

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

Secondary outcomes

  1. joint sound

    Time frame: baseline (pre treatment)

    joint sound was then determined by combining 3 means: (1) palpation of the TMJ zone by the clinician, (2) the patient's self-reporting regarding whether the joint sound could be heard, and (3) auscultation of the TMJ zone with the stethoscope.

Sponsors and collaborators

Lead sponsor

Al-Azhar University

Other

Registry information

Acronym: Posterior Disk

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Jul 7, 2021
Registry last updated
Jul 7, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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