- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01937416
Autologous Bone Marrow Mononuclear Cells Therapy in Diabetic Lower Limb Ischemia
Safety and Efficacy Investigation of Patients With Diabetic Lower Limb Ischemia by Transplantation of Autologous Bone Marrow Mononuclear Cells
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
Hebei
-
Shijiazhuang, Hebei, China, 050000
- Recruiting
- The First Hospital of Hebei Medical University
-
Contact:
- Xu Han, master
- Phone Number: 86-311-85917202
- Email: hanxu98@126.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- fontaine's stage 2-4 or resting ABI <0.7
- age between 20 and 80 years old
- sign informed consent, voluntary subjects
- diagnosis of diabetic lower limb ischemia
Exclusion Criteria:
- poorly controlled diabetes (HBA1c> 7.0%) and proliferative retinopathy (III-IV stage)
- malignancy history in the past five years or serum level of tumor markers elevated more than doubled
- severe heart, liver, kidney, respiratory failure or poor general condition can not tolerate bone marrow mononuclear cells transplantation
- serious infections (such as cellulitis, osteomyelitis, etc.)
- pregnant female, or reproductive age female who wants to give birth throughout the course of the study
- life expectancy less than half a year
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: autologous bone marrow mononuclear cells
Bone marrow come from the patients himself/herself.
With a conventional method and reagent,Ficoll, mononuclear cells were isolated with deleting erythrocyte by density gradient centrifugation.
|
Bone marrow was taken from patient oneself and mononuclear cells were isolated with deleting erythrocyte by density gradient centrifugation.
Bone marrow mononuclear cells were transplanted into ischemia regions of lower limb through intramuscular injection.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cell transplantation related side effect
Time Frame: 2 week after cell transplantation
|
Temperature,pulse,respiration,blood pressure,routine analysis of blood and urine, liver function,renal function,function of coagulation, ECG,cell transplantation related death and cell transplantation related unexpected amputation
|
2 week after cell transplantation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ulcer size
Time Frame: Post cell transplantation: 1, 3, 6 months
|
Measuring ulcer area (cm2) and depth (mm)of limb : For each ulcer , photographically record the area and depth with a ruler in order to calculate the ulcer area in square millimeters.
|
Post cell transplantation: 1, 3, 6 months
|
|
rest pain score
Time Frame: Post cell transplantation: 1,3, 6 months
|
Scoring the rest pain based on the degree of pain as following five scales): 0 level-0 point: no pain;
Before transplantation: points; after transplantation: points. |
Post cell transplantation: 1,3, 6 months
|
|
cold sensation score
Time Frame: Post cell transplantation: 1,3, 6 months
|
based on a sense of cold as following five scales: 0 level-0 point: no cold sensation;
|
Post cell transplantation: 1,3, 6 months
|
|
Resting ABI
Time Frame: Post cell transplantation: 1,3, 6 months
|
Measurement of ABI(ankle brachial index, ABI): Measure arterial pressure with a laser Doppler, and then calculate the ankle-brachial index, that is a ratio of ankle arterial blood pressure to brachial arterial blood pressure at rest.
|
Post cell transplantation: 1,3, 6 months
|
|
Resting TcPO2 (mmHg)
Time Frame: Post cell transplantation:1, 3, 6 months
|
Transcutaneous oxygen pressure(TcPO2) should be measured at the same site in the ischemic limb at rest.
|
Post cell transplantation:1, 3, 6 months
|
|
Collateral vessel score
Time Frame: Post cell transplantation: 1,3, 6 months
|
Collateral vessel score: Using computed tomographic angiography to score the collateral vessel formation. A mean score is obtained for each ischemic limb by 3 independent interventionists based on the following 4 level score: 0 (no new collateral vessels)
|
Post cell transplantation: 1,3, 6 months
|
|
Skin microcirculation measurement
Time Frame: 1,3,6 months post cell transplantation
|
using PeriMed "laser-Doppler flowmetry" measure the skin microcirculation on the same site in the ischemic limb at rest.
|
1,3,6 months post cell transplantation
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Quanhai Li, doctor, The First Hospital of Hebei Medical University
- Study Director: Huimin Zhou, doctor, The First Hospital of Hebei Medical University
- Principal Investigator: Xu Han, master, The First Hospital of Hebei Medical University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 12276102D
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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