RECRUITING

Autologous Bone Marrow Aspirate Treatment for Early-Stage Osteonecrosis

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

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.

Official Title

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

Quick Facts

Study Start:2025-04-01
Study Completion:2029-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06123481

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 to 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Lynne C Jones, PhD
CONTACT
(410) 550-4001
ljones3@jhmi.edu
Stuart Goodman, MD, PhD
CONTACT
650-721-7662
goodbone@stanford.edu

Principal Investigator

Lynne C Jones, PhD
PRINCIPAL_INVESTIGATOR
Johns Hopkins University
Michael A Mont, MD
PRINCIPAL_INVESTIGATOR
Sinai Hospital of Baltimore / LifeBridge Health
Stuart B Goodman, MD, PhD
PRINCIPAL_INVESTIGATOR
Stanford University

Study Locations (Sites)

University of Southern California
Los Angeles, California, 90033
United States
Stanford University
Stanford, California, 94063
United States
Sinai Hospital of Baltimore
Baltimore, Maryland, 21215
United States
Johns Hopkins University
Baltimore, Maryland, 21224
United States
Brigham and Women's Hospital
Boston, Massachusetts, 02115
United States
University of Minnesota
Minneapolis, Minnesota, 55455
United States
Mayo Clinic
Rochester, Minnesota, 55905
United States
NYU Langone Health Orthopedic Hospital
New York, New York, 11016
United States
Duke University
Durham, North Carolina, 27560
United States
Cleveland Clinic
Cleveland, Ohio, 441195
United States
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States
University of Virginia
Charlottesville, Virginia, 22903
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Lynne C Jones, PhD, PRINCIPAL_INVESTIGATOR, Johns Hopkins University
  • Michael A Mont, MD, PRINCIPAL_INVESTIGATOR, Sinai Hospital of Baltimore / LifeBridge Health
  • Stuart B Goodman, MD, PhD, PRINCIPAL_INVESTIGATOR, Stanford University

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 Date2025-04-01
Study Completion Date2029-07-31

Study Record Updates

Study Start Date2025-04-01
Study Completion Date2029-07-31

Terms related to this study

Keywords Provided by Researchers

  • osteonecrosis
  • aseptic necrosis
  • avascular necrosis (AVN)
  • bone marrow aspirate
  • bone marrow aspirate concentrate
  • bone marrow cells
  • bone marrow
  • cell-based treatment
  • core decompression
  • femoral head
  • necrosis
  • bone diseases
  • musculoskeletal diseases
  • pathologic processes
  • hip
  • ONFH
  • AVN

Additional Relevant MeSH Terms

  • Osteonecrosis of the Femoral Head
  • Avascular Necrosis of the Femoral Head