Comparing two surgical methods for treating meniscus extrusion
Comparison of Transtibial Pull Out Method And Suture Anchor Method in Surgical Treatment of Meniscus Extrusion
This study is testing which of two surgical methods works better for people with meniscus extrusion to improve their knee function and relieve symptoms.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 46 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Ataturk University Academic / other |
| Locations | 1 site (Erzurum, Yakutiye) |
| Trial ID | NCT06906783 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of two surgical techniques, the Transtibial Pull Out Method and the Suture Anchor Method, for treating meniscal extrusion, a condition where the meniscus is displaced beyond the tibial plateau. The study focuses on patients with meniscal extrusion greater than 3 mm, as identified through MRI scans, and aims to determine which surgical approach yields better outcomes for symptomatic patients. The trial is designed to provide insights into the optimal surgical intervention for this condition, which can significantly impact knee function.
Who should consider this trial
Good fit: Ideal candidates for this study are young, active individuals with symptomatic meniscal extrusion greater than 3 mm.
Not a fit: Patients with significant knee malalignment or advanced osteoarthritis may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and recovery for patients suffering from meniscal extrusion.
How similar studies have performed: While there is existing literature on meniscal surgery, this specific comparison of techniques is novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Presence of meniscal extrusion greater than 3 mm on MRI scans * Symptomatic complaints in the knee with extrusion Exclusion Criteria: * Malalignment greater than 5 degrees * Presence of Kellgren-Lawrence grade 3-4 osteoarthritis
Where this trial is running
Erzurum, Yakutiye
- Ataturk University Hospital — Erzurum, Yakutiye, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Muhammet Celik, primary investigator, MD
- Email: drcelik@outlook.com
- Phone: 905392087998
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.