RECRUITING

Effect of PRP, PPP, & BMAC on Functional Outcomes Following Hip Arthroscopy for Acetabular Labral Pathologies

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 goal of this clinical trial is to assess the effect of PRP/PPP/BMAC application on functional outcomes after hip arthroscopy to address acetabular labral pathologies. The main questions it aims to answer are: 1. Does PRP/PPP/BMAC application improve functional outcomes after hip arthroscopy to address acetabular labral pathologies? 2. Does PRP/PPP/BMAC application reduce the arthritic burden as measured by functional outcomes following hip arthroscopy to address labral pathologies with concomitant PRP/PPP/BMAC application?

Official Title

Effect of Platelet-Rich Plasma, Platelet-Poor Plasma, & Bone Marrow Aspirate Concentrate Application on Functional Outcomes Following Hip Arthroscopy for Acetabular Labral Pathologies: A Prospective Randomized Controlled Trial

Quick Facts

Study Start:2023-08-30
Study Completion:2045-08-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06003101

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age: \> or equal to 18 years
  2. * Clinically indicated for hip arthroscopy (by the study PI) to address a labral pathology
  3. * Willingness to participate, amenable to randomization into either treatment arm of the research study, and the ability to understand \& sign the informed consent document
  1. * Non-English speaking (PROM surveys are only validated in English)
  2. * Prior same site (i.e., ipsilateral hip) surgery, including but not limited to previous hip arthroscopy, core decompression, or periacetabular osteotomies

Contacts and Locations

Study Contact

Scott D. Martin, MD
CONTACT
617-732-5329
sdmartin@mgh.harvard.edu

Principal Investigator

Scott D. Martin, MD
PRINCIPAL_INVESTIGATOR
Massachusetts General Hospital

Study Locations (Sites)

Massachusetts General Hospital
Boston, Massachusetts, 02114
United States

Collaborators and Investigators

Sponsor: Massachusetts General Hospital

  • Scott D. Martin, MD, PRINCIPAL_INVESTIGATOR, Massachusetts General Hospital

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 Date2023-08-30
Study Completion Date2045-08-30

Study Record Updates

Study Start Date2023-08-30
Study Completion Date2045-08-30

Terms related to this study

Keywords Provided by Researchers

  • Acetabular Labrum Tear
  • Femoro Acetabular Impingement
  • Chondral Defect
  • Bone Marrow Aspirate Concentrate
  • Chondrolabral Junction
  • Osteoarthritis
  • Hip Arthroscopy
  • BMAC

Additional Relevant MeSH Terms

  • Acetabular Labrum Tear
  • Femoro Acetabular Impingement
  • Chondral Defect
  • Bone Marrow Aspirate Concentrate