RECRUITING

Knotless Implants As an Alternative for Capsular Closure in Primary Hip Arthroscopy: a Prospective, Multi-Center Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this research is to see if the Arthrex LoopLocTM device is better for capsular closure during hip arthroscopy than other treatments available. The hip capsule is the tissue that surrounds your hip joint. It stabilizes and supports your hip joint. During hip arthroscopy, this tissue must be cut through in order to perform the hip arthroscopy. Once the hip arthroscopy is completed, the surgeon might repair the capsule. Current ways of repairing the capsule include knotted suture that might irritate structures around the hip, leading to the possible formation of scar tissue and pain. The Arthrex LoopLocTM device is knotless and may lower the presence of irritation and scar tissue around the hip after surgery and might lead to better outcomes. Therefore, researchers will compare patients who had the LoopLocTM device used to close their hip capsule during surgery to those who did not have the device used, to see if there is a difference in their outcomes following surgery.

Official Title

Knotless Implants As an Alternative for Capsular Closure in Primary Hip Arthroscopy: a Prospective, Multi-Center Study

Quick Facts

Study Start:2024-10-29
Study Completion:2027-08
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06500364

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.

Ages Eligible for Study:18 Years to 60 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients undergoing a primary hip arthroscopy
  2. * Patients younger than 60 years old.
  3. * Patients who will receive capsular closure with the Arthrex LoopLocTM device following hip arthroscopy.
  1. * Patients that had previous hip surgery,
  2. * Patients that had a center edge angle (CEA) less than 25 degrees or greater than 40 degrees.
  3. * Patients that have a cartilage damage grade greater than or equal to 3.

Contacts and Locations

Study Contact

Alexandra Mantice
CONTACT
8338724477
alexandra.mantice@americanhipinstitute.org
Benjamin Domb
CONTACT
8338724477
drdomb@americanhipinstitute.org

Study Locations (Sites)

American Hip Institute Research Foundation
Des Plaines, Illinois, 60018
United States

Collaborators and Investigators

Sponsor: American Hip Institute

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-10-29
Study Completion Date2027-08

Study Record Updates

Study Start Date2024-10-29
Study Completion Date2027-08

Terms related to this study

Keywords Provided by Researchers

  • Hip arthroscopy
  • Hip capsule

Additional Relevant MeSH Terms

  • Femoro Acetabular Impingement