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

Arthroscopic Labral Repair Versus Debridement In Hip Labral Tears: A Prospective Comparative Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06288867
Enrollment
20
Registered
2024-03-01
Start date
2024-08-01
Completion date
2025-12-01
Last updated
2024-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Injuries, Acetabular Labral Tear, Femoro Acetabular Impingement

Keywords

Hip Arthroscopy, Labral Repair, Labral Debridement, Acetabular Labral Tear

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).

Interventions

Patients with Hip Labral tears will be treated with labral repair

PROCEDUREArthroscopic Labral Debridement

Patients with Hip Labral tears will be treated with labral debridement

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Hip Function, as measured by Hip Outcome Score (HOS)Baseline, 1 yearThe 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 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)
Change from baseline in Pain, as measured by the Visual Analogue Scale (VAS)Baseline, 1 yearScores 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

Countries

Egypt

Contacts

Primary ContactKarim A Salem, MD
karimatefsalem@gmail.com1000017388

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026