MedPath

A 12 Months Prospective Study Comparing Functional Outcome Scores in Hip Arthroscopic Labral Repair Versus Debridement

Not Applicable
Recruiting
Conditions
Hip Injuries
Acetabular Labral Tear
Femoro Acetabular Impingement
Interventions
Procedure: Arthroscopic Labral Repair
Procedure: Arthroscopic Labral Debridement
Registration Number
NCT06288867
Lead Sponsor
Ain Shams University
Brief Summary

This study aims to address hip labral tears and compare between arthroscopic labral repair versus debridement.

Detailed Description

Hip arthroscopy will be performed with the patient under general anesthesia. The patient will be placed in supine position, and traction and joint access will be controlled by fluoroscopy. An anterolateral portal and an inferior mid-anterior portal will be used. Any labral, chondral, and/or bony pathology (cam or pincer) will be treated. Labral tears may be debrided or repaired. Labral repairs will be secured with suture anchors.

Patient's functions will be evaluated preoperatively and postoperatively at 1, 3 and 6 months and 1 year and at the last follow-up using the Harris Hip Score (HHS), visual analog score (VAS), Hip Outcome Score Activities-Daily Living Subscale (HOS-ADL), and Sport-Specific Subscale (HOS-SSS).

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Sex: both sexes.
  • Age: 18 years - 60 years.
  • Femoroacetabular impingement (FAI) including all types (cam, pincer, and combined).
  • Traumatic Labral tears
Exclusion Criteria
  • Previous hip surgery.
  • Hip joint dysplasia, defined by both center edge (CE) angles <25 degrees and Acetabular Index angle >10 degrees.
  • Osteoarthritis grade >2 according to Tönnis classification.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Labral RepairArthroscopic Labral RepairLabral tears will be repaired with suture anchors.
Labral DebridementArthroscopic Labral DebridementLabral Debridement will be done by electrocautery
Primary Outcome Measures
NameTimeMethod
Change from baseline in Hip Function, as measured by Hip Outcome Score (HOS)Baseline, 1 year

The HOS is a patient-completed measure that consists of an "Activities of Daily Living" subscale (17 scored items) and a "Sports" subscale (9 scored items) in which the response options are presented as 5-point Likert scales (Scores 0-4). Scores for each subscale range from 0% (least function) to 100% (most function).The highest potential score is 68, a higher score represents a higher level of physical function for both the ADL and sports subscales

Change from baseline in Pain, as measured by the Visual Analogue Scale (VAS)Baseline, 1 year

Scores are measured on a 100 mm VAS. The VAS ranges from 0 to 100 with 0 indicating no pain, and higher scores indicating greater pain

Change from baseline in Hip Function, as measured by Harris Hip Score (HHS)Baseline, 1 year

\<70 (poor result), 70-79 (fair result), 80-89 (good result) and \>90 (excellent result)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ain Shams University

🇪🇬

Cairo, Egypt

© Copyright 2025. All Rights Reserved by MedPath