Effect of PRP, PPP, & BMAC on Functional Outcomes Following Hip Arthroscopy for Acetabular Labral Pathologies
{ "Hip Arthroscopy with PRP, PPP, or BMAC for Labral Tears", "This study is looking at whether adding certain biological treatments (PRP, PPP, or BMAC) during hip arthroscopy helps people recover better from hip labral tears. Hip arthroscopy is a surgery to fix problems in your hip joint, like tears in the labrum (a rim of cartilage). The study wants to see if these treatments improve how well your hip works and reduce pain over time. You might be able to join if you are at least 18 years old, need hip arthroscopy for a labral tear, and are willing to be randomly assigned to receive either the biological treatment or standard surgery. The study will measure your pain and hip function for up to two years after surgery.", "design": "This interventional study plans to enroll 160 participants who will be randomly assigned to receive either bone marrow aspirate concentrate (BMAC) during surgery or standard hip arthroscopy without it.", "commitments": "Participants will have hip arthroscopy and their pain and hip function will be measured before surgery and at 3, 6, 12, and 24 months after surgery.", "compensation": "Not stated in the trial record.", "follow_up": "Participants will be followed for 24 months after their surgery to assess their pain and hip function.", }
- Study design
- Not specified.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Not specified.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Effect of PRP, PPP, & BMAC on Functional Outcomes Following Hip Arthroscopy for Acetabular Labral Pathologies
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Scott D. Martin, MD · PRINCIPAL_INVESTIGATOR · Massachusetts General Hospital
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Pain LevelBaseline (pre-operative), 3 months, 6 months, 12 months, and 24 months
Patient Reported Outcome Measurement (PROM) to assess the patient's functional outcomes post-surgery. Range: 0-10, with 0 being no pain and 10 being the worst pain imaginable.
- Modified Harris Hip Score (mHHS)Baseline (pre-operative), 3 months, 6 months, 12 months, and 24 months
Patient Reported Outcome Measurement (PROM) to assess the patient's functional outcomes post-surgery. Scores range from 0 (poor) to 100 (ideal).
- International Hip Outcome Tool-12 (iHOT-12)Baseline (pre-operative), 3 months, 6 months, 12 months, and 24 months
Patient Reported Outcome Measurement (PROM) to assess the patient's functional outcomes post-surgery. The total score is calculated as a simple mean of these responses ranging from 0 to 100, with 100 representing the best possible quality-of-life score.
- Non-Arthritic Hip Score (NAHS)Baseline (pre-operative), 3 months, 6 months, 12 months, and 24 months
Patient Reported Outcome Measurement (PROM) to assess the patient's functional outcomes post-surgery. Scores range from 0 (poor) to 100 (ideal).
- Hip Outcome Score (HOS)Baseline (pre-operative), 3 months, 6 months, 12 months, and 24 months
Patient Reported Outcome Measurement (PROM) to assess the patient's functional outcomes post-surgery. Scores range from 0 (poor) to 100 (ideal).
- Kerlan-Jobe Orthopaedic Clinic Athletic Hip ScoreBaseline (pre-operative), 3 months, 6 months, 12 months, and 24 months
Patient Reported Outcome Measurement (PROM) to assess the patient's functional outcomes post-surgery. Scores range from 0 (poor) to 100 (ideal).
- Visual Analog Scale (VAS) Pain ScoreBaseline (pre-operative), 3 months, 6 months, 12 months, and 24 months
Patient Reported Outcome Measurement (PROM) to assess the patient's functional outcomes post-surgery. Range: 0-10, with 0 being no pain and 10 being the worst pain imaginable.