Autologous Bone Marrow Aspirate Treatment for Early-Stage Osteonecrosis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorJohns Hopkins University

About this trial

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 criteria

Qualifiers

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

Disqualifiers

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

Sickle Cell disease

Trial design

Treatments tested in this trial

  • Core Decompression
  • Core Decompression Procedure with Autologous Bone Marrow Aspirate Concentrate

Treatment groups

192 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Johns Hopkins University

Lead sponsor

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Collaborator