Actively Recruiting
Prospective Randomized Control Trial Comparing Absorbable Sutures to Non-Absorbable Sutures for Capsular Closures in Hip Arthroscopies
Led by University of Missouri-Columbia · Updated on 2025-05-04
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating absorbable sutures compared to non-absorbable sutures used for capsular repair during hip arthroscopic procedures. This study aims to assess how these suture types affect hip function and recovery in patients with hip joint injuries such as labrum injury, femoroacetabular impingement syndrome, and those undergoing hip arthroscopy. Major outcomes will be measured with patient questionnaires and radiographic imaging to monitor healing and complications. The study involves two groups receiving either absorbable or non-absorbable sutures for hip capsular closure during surgery. Participants will complete several questionnaires including the International Hip Outcome Tool-12, modified Harris hip score, and hip outcome score, as well as nine standard care questionnaires at multiple time points: before surgery, and at 6 weeks, 3 months, 6 months, 1 year, 2 years, and any other follow-up visits. Radiographs taken as part of standard care will be used to evaluate heterotrophic ossification at 6 months after surgery. Participants will be monitored through surveys assessing hip function, pain, activity, and surgical satisfaction, along with radiographic imaging at follow-up visits. The main outcomes measure changes in hip-related quality of life and function up to 12 months post-surgery. Safety and healing will be monitored through imaging at 6 months. The total participation duration may extend to 2 years or more, depending on follow-up visits.
CONDITIONS
Brief Title
Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects 18 years of age and older
- Subject requiring surgical hip arthroscopic intervention for their hip pathology
You will not qualify if you...
- Subjects less than 18 years of age
- Subjects with any other medical problem precluding anesthesia or surgery
- Unable to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Day of surgery and immediate recovery period
Participants undergo hip arthroscopic surgery with either absorbable or non-absorbable sutures for capsular closure.
1 surgery visit (in-person)
Duration - Up to 2 years
Participants attend follow-up visits to complete standard of care questionnaires and undergo radiographic imaging to assess recovery and surgical outcomes.
Visits at preoperative, 6 weeks, 3 months, 6 months, 1 year, and 2 years
Trial Site Locations
Total: 1 location
1
Missouri Orthopaedic Institute
Columbia, Missouri, United States, 65201
Actively Recruiting
Research Team
V
Vicki Jones, MEd, CCRP
T
Trever T Simon
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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