Skip to main content
Clinical Trials/NCT00557635
NCT00557635
Suspended
Phase 2

Osseous Setting Improvement With Co-implantation of Osseous Matrix and Mesenchymal Progenitors Cells From Autologous Bone Marrow

University Hospital, Clermont-Ferrand0 sites50 target enrollmentJanuary 2008

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Tibia or Femur Pseudo-arthrosis
Sponsor
University Hospital, Clermont-Ferrand
Enrollment
50
Primary Endpoint
Evaluate osseous setting at 3-months follow-up and compare our results with past studies
Status
Suspended
Last Updated
16 years ago

Overview

Brief Summary

Sometime osseous reconstruction needs allogeneic bone, in this study we use Ostéopure™ from Ostéobanque d'Auvergne, which is a osseous matrix. However Ostéopure™ integration lasts a long time. To optimize this integration we purpose to associate mesenchymal progenitors cells from autologous bone marrow.

Detailed Description

All patients will be treated for tibia or femur pseudo-arthrosis. At the beginning of chirurgical intervention, autologous bone marrow will be sampling and will be concentrated during this one. Meanwhile osseous matrix (Ostéopure™ ) will be incubated in autologous blood serum and finally implanted in the fracture site. And after (at the end of chirurgical intervention), concentrate autologous bone marrow will be injected in the same place.

Registry
clinicaltrials.gov
Start Date
January 2008
End Date
December 2011
Last Updated
16 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Clermont-Ferrand

Eligibility Criteria

Inclusion Criteria

  • tibia or femur pseudo-arthrosis,
  • patient who needs bone graft

Exclusion Criteria

  • - contra indications for chirurgical intervention or bone graft

Outcomes

Primary Outcomes

Evaluate osseous setting at 3-months follow-up and compare our results with past studies

Time Frame: at 3-months follow-up

Secondary Outcomes

  • Feasibility and tolerance of this therapeutic strategy(at 3-months follow-up)

Similar Trials