Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06845735

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects 18 years of age and older
  • Subject requiring surgical hip arthroscopic intervention for their hip pathology
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

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)

Post-operative Follow-up

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

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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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