Assessment of Concentric Needle Technique in Temporomandibular Joint (TMJ) Internal Derangement.

NCT ID: NCT05510336

Last Updated: 2022-08-22

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-01

Study Completion Date

2022-12-01

Brief Summary

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The aim of the study is to evaluate the effectivenes of using two concentric needles in comaprsion with the normal traditional two distant needles.

Detailed Description

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Conditions

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TMJ Disc Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Study group

Concentric needle technique TMJ arthrocentesis using lactated ringer solution to help reduce inflammatory mediators and anterior disc discplacement with reduction

Group Type ACTIVE_COMPARATOR

Arthrocentesis

Intervention Type PROCEDURE

Injection of lactated ringer solution in the TMJ to wash out inflammatory mediators and help reducing anterior disc displacement with reduction

Control group

Double needle technique TMJ arthrocentesis using lactated ringer solution to help reduce inflammatory mediators and anterior disc discplacement with reduction

Group Type ACTIVE_COMPARATOR

Arthrocentesis

Intervention Type PROCEDURE

Injection of lactated ringer solution in the TMJ to wash out inflammatory mediators and help reducing anterior disc displacement with reduction

Interventions

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Arthrocentesis

Injection of lactated ringer solution in the TMJ to wash out inflammatory mediators and help reducing anterior disc displacement with reduction

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Patients with age ranges from 18-60.
2. Patients with painful clicking.
3. Patients free of systemic conditions that might affect the TMJ or interfere with carrying out the surgical procedure (osteoarthritis, rheumatoid arthritis, uncontrolled diabetes).

Exclusion Criteria

1. Patients out of the specified range group
2. Patients with painless TMJ clicking.
3. Patients with osteo-arthritic changes of the TMJ.
4. Patients with systemic conditions that might affect the TMJ or interfere with carrying out the surgical procedure (osteoarthritis, rheumatoid arthritis, uncontrolled diabetes).
5. Patients with previous TMJ surgeries.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Ahmed Adel Hassan Mahmoud

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Ahmed Adel, BDS Dentistry

Role: CONTACT

01229530562

Nesrine Khairy, PHD Maxillofacial surgery

Role: CONTACT

01002714479

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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Concentric needle technique

Identifier Type: -

Identifier Source: org_study_id

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