Sutures for Hip Arthroscopy
Trial Summary
What is the purpose of this trial?
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.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What data supports the effectiveness of the treatment Sutures for Hip Arthroscopy?
Is the use of sutures in hip arthroscopy generally safe?
How do absorbable and non-absorbable sutures differ in hip arthroscopy treatment?
Absorbable sutures dissolve over time and are absorbed by the body, which can be beneficial for reducing the need for suture removal, while non-absorbable sutures remain in the body and may provide longer-lasting support but might require removal if they cause irritation or complications. The choice between these sutures can affect healing, patient satisfaction, and the risk of complications, as seen in other procedures like knee and Achilles tendon repairs.910111213
Eligibility Criteria
This trial is for individuals with a hip labral tear or femoroacetabular impingement who are undergoing hip arthroscopy. Participants should be suitable candidates for the procedure and willing to complete follow-up questionnaires.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Preoperative Assessment
Participants complete preoperative questionnaires and assessments
Treatment
Participants undergo hip arthroscopic procedures with either absorbable or non-absorbable sutures
Postoperative Follow-up
Participants are monitored postoperatively with questionnaires and radiographic assessments
Treatment Details
Interventions
- Absorbable Suture
- Non-Absorbable Sutures
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Missouri-Columbia
Lead Sponsor