RecruitingNot ApplicableNCT06123481

Autologous Bone Marrow Aspirate Treatment for Early-Stage Osteonecrosis

Autologous Bone Marrow Aspirate Concentrate for the Treatment of Osteonecrosis of the Femoral Head


Sponsor

Johns Hopkins University

Enrollment

192 participants

Start Date

Apr 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Osteonecrosis of the femoral head (ONFH) is a debilitating musculoskeletal disease that is characterized by localized death of bone cells and associated cellular elements within the subchondral bone. If it progresses, it results in the collapse of the femoral head (ball part of the hip) giving rise to secondary arthritis. This condition is associated with marked pain and loss of function, often necessitating a joint replacement. Due to the relatively young age of onset of ONFH (often in 20s and 30s), there is great interest in utilizing joint-preserving procedures prior to the need for joint replacement. Joint-preserving procedures include core decompression (CD) with and without bone grafts or cells, vascularized and non-vascularized bone grafting, as well as osteotomies. Inconsistent results for each of these procedures have been reported and there are no Clinical Practice Guidelines or medical community consensus opinions regarding the treatment of early-stage ONFH. The hypothesis to be tested is "Participants who have early-stage ONFH undergoing CD augmented with autogenous bone marrow aspirate concentrate will have better clinical and radiological outcomes than CD alone." This multi-center randomized controlled trial for early-stage ONFH is prospective and controlled for participant stage (only early-stage pre-collapse individuals) and surgical technique. Participants will be evaluated as per routine surgical follow-up, and at 6 months (telemedicine), 1- and 2- years using radiographs, MRIs, and questionnaires. This project will also explore the scientific basis for success vs. failure in individuals who have osteonecrosis, and have different demographics and bone marrow aspirate cell profiles.


Eligibility

Min Age: 18 YearsMax Age: 90 Years

Inclusion Criteria4

  • Participants who have non-traumatic osteonecrosis of the femoral head
  • Only participants who have Stage 1 or 2 osteonecrosis as assessed by the 2019 ARCO Staging System
  • No evidence of subchondral fracture
  • All osteonecrotic lesion sizes

Exclusion Criteria15

  • Participants diagnosed who have femoral head osteonecrosis for which no risk factor has yet to be identified
  • Participants will include all ethnicities and races
  • Be able and willing to participate in study and return for postoperative visits
  • Participants who have:
  • Sickle Cell disease
  • Major trauma
  • Post-irradiation ON
  • Gaucher Disease
  • Juvenile form: Legg-Calve-Perthes Disease
  • Juvenile form: Spontaneous ON of the hip
  • Pregnant or breastfeeding
  • Vulnerable population; i.e., prisoners and institutionalized individuals
  • Participant is unable to undergo an MRI
  • Participants who have evidence of a subchondral fracture
  • Prior history of hip surgery, more extensive than hip arthroscopy

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Interventions

PROCEDURECore Decompression

Standard core decompression procedure is performed by drilling into the necrotic bone of the femoral head. A sham bone marrow aspiration involves advancing a needle to the iliac crest (no bone penetration, no bone marrow aspiration) through a small skin incision.

PROCEDURECore Decompression Procedure with Autologous Bone Marrow Aspirate Concentrate

This involves bone marrow aspiration, concentrating the bone marrow aspirate, and injecting 6 milliliters of bone marrow aspirate concentrate into the necrotic femoral head through an opening created by the core decompression.


Locations(10)

University of Southern California

Los Angeles, California, United States

Stanford University

Stanford, California, United States

Sinai Hospital of Baltimore

Baltimore, Maryland, United States

Johns Hopkins University

Baltimore, Maryland, United States

University of Minnesota

Minneapolis, Minnesota, United States

Mayo Clinic

Rochester, Minnesota, United States

NYU Langone Health Orthopedic Hospital

New York, New York, United States

Cleveland Clinic

Cleveland, Ohio, United States

University of Pennsylvania

Philadelphia, Pennsylvania, United States

University of Virginia

Charlottesville, Virginia, United States

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NCT06123481


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