Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure
Part of paid clinical trials in Columbia, Missouri.
- Sponsor
- University of Missouri-Columbia
- Study ID
- NCT06845735
- Status
- Recruiting
Conditions
- Femoroacetabular Impingement Syndrome
- Hip Arthroscopy
- Labrum Injury of the Hip Joint
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Non-Absorbable Sutures — DEVICENon-Absorbable Sutures
- Absorbable Suture — DEVICEAbsorbable suture
Study Details
The study is to prospectively compare absorbable sutures with non-absorbable sutures used for capsular repair during hip arthroscopic procedures. Major outcomes will be measured using three questionnaires ((1) International Hip Outcome Tool-12 (iHOT-12), (2) modified Harris hip score, (3) hip outcome score) in addition to the standard of care set of 9 questionnaires. The other major outcome will be any radiographic heterotrophic ossification at the 6-month follow-up time point.
Key Dates
- Start date
- Mar 22, 2024
- Status verified
- Apr 2025
- Primary completion
- Jan 1, 2028
- Completion
- Jan 1, 2028
Study Design
- Enrollment
- 100 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Absorbable SutureAbsorbable suture
- Active Comparator: Non-Absorbable SutureNon-Absorbable Sutures
Primary Outcome Measure
International Hip Outcome Tool-12 (IHOT-12) [ Time Frame: Preoperative to 12 months postoperative ]
Central Contacts
- Vicki Jones, MEd, CCRP573-882-7583
- Trever T Simon573-882-1403
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Missouri Orthopaedic Institute | Columbia | Missouri | 65201 | Steven F DeFroda, MD, MEng (PRINCIPAL_INVESTIGATOR) |
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