Treatment of Atrophic Nonunion by Preosteoblast Cells
Primary Purpose
Pseudarthrosis, Fractures, Ununited
Status
Completed
Phase
Phase 1
Locations
Belgium
Study Type
Interventional
Intervention
percutaneous autologous preosteoblast cells implantation
Sponsored by
About this trial
This is an interventional treatment trial for Pseudarthrosis focused on measuring pseudarthrosis, Treatment, osteoblast grafting, cell therapy, nonunion
Eligibility Criteria
Inclusion Criteria:
- Fracture of a long bone having insufficient healing after minimum 6 months.
- Be able and willing to participate in the study.
Exclusion Criteria:
- Evidence of malignant disorder in the past five year.
- Patient who is positive for an HIV, hepatitis B or C infection.
- Insufficient reduction of the fracture with displaced fragments.
- Evidence of local sepsis by biological parameters and/or positive isotopic scan using leucocytes labelled by Indium.
Sites / Locations
- CHU Sart Tilman
Outcomes
Primary Outcome Measures
radiological progression of bone fusion
monthly
Secondary Outcome Measures
reduction of pain using VAS
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00916981
Brief Title
Treatment of Atrophic Nonunion by Preosteoblast Cells
Official Title
Treatment of Refractory Non-union Fractures by Pre-osteoblast Cells Grafting : a Pilot Study.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
June 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jean-Philippe Hauzeur
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Treatment of nonunion, delayed union and malunion fractures of long bones remains problematic. The definition of nonunion is a failure of the fracture to heal in six months in a patient in whom progressive repair had not been observed radiographically between the third and sixth month after the fracture. First of all good surgical techniques are stable immobilization must be obtained and local sepsis excluded. Then stimulation of the callus is required. Numerous techniques have been developed ranging from invasive interventions (including internal fixation with the use of bone graft or bone graft substitutes) to non invasive procedures (ultrasound and pulsed electromagnetic fields).
Recently, autologous cell therapy was presented as an interesting approach. The concept of such therapies is based on the effect of stem cells presented in the bone marrow and able to be transformed in osteoblast cells. The percutaneous technique of autologous bone-marrow grafting is a minimally invasive alternative able to produce a good healing of the fracture. The efficacy is dependent of the concentration in progenitor cell reinjected. An optimization of this type of treatment could be achieved using a technique to increase the differentiation of the bone marrow cells in preosteoblasts before the injection in situ by an adequate culture. Therefore we would like to start a pilot open study on the feasibility and the efficacy of implantation of preosteoblasts into nonunion. Two different presentations exist: the atrophic and the hypertrophic pseudarthrosis in relationship with radiological features of bone proliferation at the tip of bone fragments. Some data support that atrophic and hypertrophic nonunion fractures could have different physiopathological factors. So, in a first time we only would evaluate the atrophic form and to determine in an open study the effect of the implantation of preosteoblasts into atrophic nonunion.
Detailed Description
We will recruit 30 patients having a atrophic nonunion fracture of long bone present for minimum 6 months.50 ml of bone marrow harvest will be performed under local anaesthesia 3 weeks before the implantation. After three weeks of culture, preosteoblastic cells will be injected into the site of pseudarthrosis under radioscopic control, using percutaneously a 3 mm trephine.
An immobilization and non weight-bearing of the bone will be respected during the first month after the injection. If callus could be observed on radiographs, partial mobilization and weight-bearing will be allowed during the second month.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pseudarthrosis, Fractures, Ununited
Keywords
pseudarthrosis, Treatment, osteoblast grafting, cell therapy, nonunion
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
percutaneous autologous preosteoblast cells implantation
Other Intervention Name(s)
PREOB
Intervention Description
percutaneously injection of preosteoblast into the nonunion under radioscopic control
Primary Outcome Measure Information:
Title
radiological progression of bone fusion
Description
monthly
Time Frame
1, 2, 3, 4, 5, 6 months
Secondary Outcome Measure Information:
Title
reduction of pain using VAS
Time Frame
each month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Fracture of a long bone having insufficient healing after minimum 6 months.
Be able and willing to participate in the study.
Exclusion Criteria:
Evidence of malignant disorder in the past five year.
Patient who is positive for an HIV, hepatitis B or C infection.
Insufficient reduction of the fracture with displaced fragments.
Evidence of local sepsis by biological parameters and/or positive isotopic scan using leucocytes labelled by Indium.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Philippe Hauzeur, MD, PhD
Organizational Affiliation
University of Liège, Belgium
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Sart Tilman
City
Liege
State/Province
Liège
ZIP/Postal Code
4000
Country
Belgium
12. IPD Sharing Statement
Learn more about this trial
Treatment of Atrophic Nonunion by Preosteoblast Cells
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