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Clinical Trials/NCT01788059
NCT01788059
Completed
Phase 2

The Efficacy of Mesenchymal Stem Cells for Stimulate the Union in Treatment of Non-united Tibial and Femoral Fractures in Shahid Kamyab Hospital

Emdadi Kamyab Hospital1 site in 1 country19 target enrollmentJanuary 2013

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Nonunion Fracture
Sponsor
Emdadi Kamyab Hospital
Enrollment
19
Locations
1
Primary Endpoint
clinical and radiological union at 1 month to 6 months
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Because the rate of non union of long bone in lower extremities specially in tibia in this two last decade due to malnutrition and smoking and other risk factors was increased, so many patient in our country suffer from non union on the other hand it seems that the use of the mesenchymal stem cells can irritate the union rate. Therefore the investigators decide to inject the mesenchymal stem cell derived from iliac bone marrow after centrifuge with ficoll procedure to non union site in patient that are resistant to other treatment. Then the investigators will follow the patient with monthly radiography and evaluate the callus volume and clinical union and any side effect of this treatment.clinical union consider to relief pain in non union site and be stable in examination.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
November 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Emdadi Kamyab Hospital
Responsible Party
Principal Investigator
Principal Investigator

mohammad taghi peivandi

MD

Emdadi Kamyab Hospital

Eligibility Criteria

Inclusion Criteria

  • Every patient with non union in the site of long bone fracture
  • Age more than 18 and under 60 years old
  • Fracture having no radiological callus after 6 months and absence of any hypertrophic bone reaction.
  • No infection in site of surgery
  • Be able and willing to participate in the study
  • Written informed consent

Exclusion Criteria

  • Evidence of malignancy
  • Pregnancy or breastfeeding
  • Patient positive by serology or PCR for HIV, hepatitis B or C infection the patient with Accompanied fracture such as hip fracture that could not weight bearing

Outcomes

Primary Outcomes

clinical and radiological union at 1 month to 6 months

Time Frame: 6 months

patients receiving Mesenchymal Stem Cells that develop a partial or complete callus at 1, 2, 3, 4 ,5 and 6 months evaluate with standard X-rays

Secondary Outcomes

  • •Safety of Mesenchymal Stem Cells injection in nonunion fractures. Follow-up for revealing any significant immediate or late adverse effects.(12 months)
  • Incidence of adverse events in patients (e.g infection , malignancy , ...) Adverse events will be continuously monitored(12 months)

Study Sites (1)

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