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Clinical Trials/NCT01429012
NCT01429012
Withdrawn
Phase 2

Treatment of Atrophic Nonunion Fractures by Autologous Mesenchymal Stem Cell Percutaneous Grafting. A Randomized, Double-blind, Controlled Study

University of Liege1 site in 1 countryNovember 2012

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Nonunion Fracture
Sponsor
University of Liege
Locations
1
Primary Endpoint
Proportion of patients receiving Mesenchymal Stem Cells that develop a partial or complete callus at 6 and 12 months, compared to patients receiving placebo.
Status
Withdrawn
Last Updated
4 years ago

Overview

Brief Summary

Bone fractures heal most of the time particularly well and without complications. The solidification takes rarely more than two to three months. The wound healing depends greatly on a good blood supply and needs several steps. These processes culminate in a new mass of heterogeneous tissue which is known as the fracture callus. Unfortunately, 2%-5% bone fractures cannot achieve a proper solidification and between the ununited fragments a scar tissue appears. This incorrect healing induces pain and even infections. When this situation persists more than 6 months, it is referred to as nonunion fracture, which will require some form of intervention to stimulate the natural healing process of the body. First of all, good surgical techniques with stable immobilization should be applied and local infection should be excluded. Then stimulation of the callus is required. Cell therapy with bone marrow cells has emerged as a promising new approach for bone regeneration. Animal studies as well as preliminary human studies have shown that Mesenchymal Stem Cells, a particular kind of stem cells isolated from the bone marrow, could induce callus formation when injected in the nonunion site of a broken bone.

In this study the investigators aim at determining whether Mesenchymal Stem Cells (MSC) isolated from the patient's bone marrow and injected in the nonunion site could be a safe and effective treatment for nonunion fractures. Patients will be randomized in two groups; one injected with Mesenchymal Stem Cell and the other injected with placebo. The investigators seek also to know how long it takes to develop the callus formation and whether there is a partial or a complete callus formation.

Registry
clinicaltrials.gov
Start Date
November 2012
End Date
November 2016
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yves Beguin

MD, PhD

University of Liege

Eligibility Criteria

Inclusion Criteria

  • Male or female; female patients must use a reliable contraception method
  • Age ≥ 18 years
  • Fracture having no radiological callus after 6 months and absence of any hypertrophic bone reaction.
  • No sepsis
  • Good skin covering
  • Be able and willing to participate in the study
  • Written informed consent

Exclusion Criteria

  • Evidence of malignancy (except non-melanoma skin cancer) in the past five years
  • Pregnancy or breastfeeding
  • Patient positive by serology or PCR for HIV, hepatitis B or C infection
  • Insufficient reduction of the fracture with displaced fragments
  • Evidence of local sepsis by clinical signs, biological parameters (CRP) and/or positive isotopic scan using Indium-labelled leucocytes

Outcomes

Primary Outcomes

Proportion of patients receiving Mesenchymal Stem Cells that develop a partial or complete callus at 6 and 12 months, compared to patients receiving placebo.

Time Frame: 6 and 12 months

Radiological evaluation of the callus by standard X-rays and computed tomography (CT).

Safety of Mesenchymal Stem Cells injection in nonunion fractures.

Time Frame: 12 months

Follow-up for revealing any significant immediate or late adverse effects.

Secondary Outcomes

  • Value of [18F]-NaF PET scans for early prediction of the onset of the bone healing process.(3 months)
  • Timing of development of a partial or complete callus in the 2 groups.(12 months for one injection or 18 months when a second injection is needed)
  • Proportion of patients receiving Mensechymal Stem Cells that develop a partial or complete callus at 2, 3, 4, 8 and 10 months, compared to patients receiving placebo(2, 3, 4, 8 and 10 months)
  • Patient evaluation of pain and global satisfaction.(12 months)
  • Proportion of patients achieving different degrees of functional success.(2, 3, 4, 6, 8, 10 and 12 months)
  • Evaluation of early homing of Mesenchymal Stem Cells.(24 hours)
  • Incidence of adverse events and severe adverse events in the 2 groups.(12 months for one injection and 18 months when a second injection is performed)

Study Sites (1)

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