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Clinical Assessment of the Efficacy and Safety of a New-Generation Temporomandibular Joint Arthroscope in TMJ Surgery

Clinical Assessment of the Efficacy and Safety of a New-Generation Temporomandibular Joint Arthroscope in TMJ Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102765
Enrollment
Unknown
Registered
2025-05-20
Start date
2025-05-22
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Temporomandibular Joint Disorders

Interventions

The domestic temporomandibular joint arthroscopy surgery team:Under general anesthesia, the temporomandibular joint (TMJ) arthroscopy was performed using a double-puncture technique. The synovium and

Sponsors

West China Hospital of Stomatology Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-45 years, regardless of gender; 2. MRI-confirmed diagnosis of temporomandibular joint disc displacement without reduction, with disc length = anteroposterior diameter of the condyle; 3. Disease duration >3 months, presenting with at least one of the following: joint pain, audible sounds, or abnormal mandibular movement; 4. Patients informed and consented to participate in the study; 5. Willing to undergo arthroscopic disc repositioning surgery of the temporomandibular joint (5 cases total).

Exclusion criteria

Exclusion criteria: 1. Patients who have previously undergone treatment for temporomandibular joint disorders (TMD); 2. Patients with concurrent infections, tumors, trauma, or other systemic diseases; 3. Patients with jaw deformities, dentition defects, unstable occlusion, or severe occlusal dysfunction; 4. Patients with disc length shorter than the anteroposterior diameter of the condyle, severe disc deformation, or perforation, making disc surgery unfeasible; 5. Patients with immune system disorders, such as rheumatoid arthritis; 6. Pregnant or lactating women, or women planning pregnancy during the study period.

Design outcomes

Primary

MeasureTime frame
Non-conversion rate of surgery;Visualization quality of the surgical field;

Secondary

MeasureTime frame
Surgeon's satisfaction level;Volume of intraoperative hemorrhage;Visual Analog Scale (VAS) pain scores;Incidence of complications;

Countries

China

Contacts

Public ContactSongsong Zhu

West China Hospital of Stomatology Sichuan University

zss_1977@163.com+86 28 8550 3530

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026