Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure

Description

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.

Conditions

Labrum Injury of the Hip Joint, Hip Arthroscopy, Femoroacetabular Impingement Syndrome

Study Overview

Study Details

Study overview

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.

Prospective Randomized Control Trial Comparing Absorbable Sutures to Non-Absorbable Sutures for Capsular Closures in Hip Arthroscopies

Absorbable vs Non-Absorbable Sutures for Hip Capsular Closure

Condition
Labrum Injury of the Hip Joint
Intervention / Treatment

-

Contacts and Locations

Columbia

Missouri Orthopaedic Institute, Columbia, Missouri, United States, 65201

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Subjects 18 years of age and older.
  • * Subject requiring surgical hip arthroscopic intervention for their hip pathology
  • * Subjects less than 18 years of age.
  • * Subjects with any other medical problem precluding anesthesia or surgery.
  • * Unable to provide informed consent.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Missouri-Columbia,

Study Record Dates

2028-01-01