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Comparative Assessment of Arthrocentesis Methods in TMJ Disorders

H

Helin Merve Özalp

Status

Completed

Conditions

Temporomandibular Disorders (TMD)
Temporomandibular Joint Disc Displacement, With Reduction

Treatments

Procedure: Y-shaped cannula with a source
Procedure: Y-shaped cannula without a source

Study type

Interventional

Funder types

Other

Identifiers

NCT07327099
KTU-DHF-HMO-01

Details and patient eligibility

About

Temporomandibular disorders (TMD) are common conditions in society, characterised by symptoms such as pain, limited movement and joint noises, which negatively affect an individual's quality of life. The primary goal of treatment is to restore the physiological functions of the joint by eliminating the aetiological factors. In cases where conservative methods prove ineffective, arthrocentesis, a minimally invasive approach, comes to the fore. Arthrocentesis aims to reduce pain by removing inflammatory mediators and to increase joint mobility. In this study, the intraoperative parameters and clinical outcomes of different arthrocentesis techniques were compared and evaluated in patients with Wilkes stage 2-3 TME disorders.

Full description

Introduction: Temporomandibular disorders (TMD) are common symptoms in society, characterized by pain, limited movement, and all sounds, which are often negatively impacted by individual life circumstances. The primary goal of treatment is to eliminate the etiological factors and restore the replaceable functions of the parts. Arthrocentesis, a minimally invasive approach, is emphasized in cases where conservative treatment is beneficial. Arthrocentesis reduces pain by removing inflammatory mediators and increases joint mobility. This effective treatment was evaluated by comparing the intraoperative parameters and clinical success of different arthrocentesis techniques in patients with Wilkes stage 2-3 TMJ disorders.

Materials and Methods: This study is being conducted at the Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Karadeniz Technical University. Fifty patients (Group 1: n=25, Group 2: n=25) treated with two different arthrocentesis technologies were enrolled retrospectively. The first group was the study of Mun et al. Arthrocentesis was performed using the method employed by Rahal et al., which consisted of two 22-gauge needles bent to form a "Y" shape and placed simultaneously and concentrically. The second group underwent arthrocentesis using a fabricated Y-shaped cannula used by Rahal et al. Each treatment was performed under local anesthesia, and the upper regions were irrigated with an average of 100 ml of Ringer's lactate solution. Following arthrocentesis, 1 ml of hyaluronic acid was injected into the patients. Preoperative and postoperative values were evaluated by comparing the groups at 1 to 6 months. Furthermore, intraoperative arthrocentesis efficiency (number of needle insertions, procedure time, complication rate, and treatment tolerance) was compared between the groups.

Enrollment

50 patients

Sex

All

Ages

17 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with unilateral TME disorders who:

  • Are in stages 2-3 of the Wilkes classification
  • Have not undergone interventional treatment prior to arthroscopy
  • Have undergone conservative treatment prior to arthroscopy without successful results

Exclusion criteria

  • Patients with TME irregularities who have undergone interventional treatment (minimally invasive and invasive)
  • Patients with bilateral TME disorders
  • Patients with incomplete recorded data

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

group 1
Active Comparator group
Description:
The first group underwent arthrocentesis using a method developed by Mun et al., involving two 22-gauge needles bent to form a Y-shape with their angles facing each other.
Treatment:
Procedure: Y-shaped cannula without a source
group 2
Active Comparator group
Description:
The second group underwent arthrocentesis using a method developed by Rahal et al., involving a factory-made Y-shaped cannula.
Treatment:
Procedure: Y-shaped cannula with a source

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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