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Comparing Two-Needle vs. Surgery-Guided Arthrocentesis for TMJ Disorders

M

Marmara University

Status

Completed

Conditions

Temporomandibular Joint Disorders

Treatments

Procedure: Surgery-Guided Arthrocentesis
Procedure: Traditional Two-Needle Arthrocentesis

Study type

Interventional

Funder types

Other

Identifiers

NCT06055855
MUDHF_FB_007

Details and patient eligibility

About

The goal of this clinical trial is to compare two methods of arthrocentesis in treating temporomandibular joint (TMJ) disorders. The main questions it aims to answer are:

Is surgery-guided arthrocentesis more efficient in terms of operation time compared to traditional two-needle arthrocentesis? Does the use of surgical guides lead to less postoperative pain and better patient comfort?

Participants will:

Undergo either the traditional two-needle arthrocentesis or the surgery-guided arthrocentesis.

Be monitored for operation time, postoperative pain, and overall patient comfort.

Researchers will compare the outcomes of patients who underwent traditional two-needle arthrocentesis with those who had surgery-guided arthrocentesis to see if the latter can shorten operation time and improve patient comfort.

Enrollment

20 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with Wilkes stage II, III, or IV Temporomandibular Joint (TMJ) internal derangement.
  • Presence of pain, sound, or both in the TMJ.
  • Limitation or locking in mouth opening, or both.
  • Patients who have not responded to symptoms after a minimum of three months of splint therapy.

Exclusion criteria

  • Presence of infection in the puncture area.
  • Presence of osteomyelitis in the neighboring region.
  • Patients with uncontrolled coagulopathies.
  • Patients experiencing limitation in maximum mouth opening without disk disorder.
  • Patients with severe degenerative joint disease (e.g., deformed condylar contour, osteophyte findings in MRI).
  • History of TMJ surgery.
  • History of muscle-originated mandibular hypomobility.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

20 participants in 2 patient groups

Traditional Arthrocentesis Group
Active Comparator group
Treatment:
Procedure: Traditional Two-Needle Arthrocentesis
Surgery-Guided Arthrocentesis Group
Experimental group
Treatment:
Procedure: Surgery-Guided Arthrocentesis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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