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

Primary Purpose

Nonunion Fracture

Status
Completed
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
injection the mesenchymal stem cell in non union site
Sponsored by
Emdadi Kamyab Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonunion Fracture focused on measuring nonunion, mesenchymal stem cell, long bone

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Emdai Kamyab Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

mesenchymal stem cell

Arm Description

stem cells drived from iliac bone marrow with centrifuge and ficoll method then inject to non union site 2-3 ml with approximately 40 X 10E6 Mesenchymal Stem Cells (MSC) will be injected in the nonunion site of the bone fracture under fluoroscopic gide and general or spinal anesthesia as deemed appropriate by the anesthetist.

Outcomes

Primary Outcome Measures

clinical and radiological union at 1 month to 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 Outcome Measures

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

Full Information

First Posted
January 17, 2013
Last Updated
December 26, 2013
Sponsor
Emdadi Kamyab Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01788059
Brief Title
The Efficacy of Mesenchymal Stem Cells for Stimulate the Union in Treatment of Non-united Tibial and Femoral Fractures in Shahid Kamyab Hospital
Official Title
The Efficacy of Mesenchymal Stem Cells for Stimulate the Union in Treatment of Non-united Tibial and Femoral Fractures in Shahid Kamyab Hospital
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
October 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emdadi Kamyab Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonunion Fracture
Keywords
nonunion, mesenchymal stem cell, long bone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
mesenchymal stem cell
Arm Type
Experimental
Arm Description
stem cells drived from iliac bone marrow with centrifuge and ficoll method then inject to non union site 2-3 ml with approximately 40 X 10E6 Mesenchymal Stem Cells (MSC) will be injected in the nonunion site of the bone fracture under fluoroscopic gide and general or spinal anesthesia as deemed appropriate by the anesthetist.
Intervention Type
Other
Intervention Name(s)
injection the mesenchymal stem cell in non union site
Primary Outcome Measure Information:
Title
clinical and radiological union at 1 month to 6 months
Description
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
Time Frame
6 months
Secondary Outcome Measure Information:
Title
•Safety of Mesenchymal Stem Cells injection in nonunion fractures. Follow-up for revealing any significant immediate or late adverse effects.
Time Frame
12 months
Title
Incidence of adverse events in patients (e.g infection , malignancy , ...) Adverse events will be continuously monitored
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
mohammad taghi peivandi, MD
Organizational Affiliation
Emdadi Kamyab Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emdai Kamyab Hospital
City
Mashhad
State/Province
Khorasan
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Learn more about this trial

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

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