Diabetic Foot Clinical Trial
Official title:
Comparison of Autologous Transplantation of Bone Marrow Mesenchymal Stem Cells and Mononuclear Cells on Diabetic Critical Limb Ischemia and Foot Ulcer
Objective:
To compare the effect and safety of autologous transplantation of bone marrow mesenchymal
stem cells(MSCs) and mononuclear cells(MNCs) on Diabetic patients with Critical Limb
Ischemia and Foot Ulcer.
Methods:
patients were randomized into the A group and the B group by use of a randomization table.
One lower limb in A group or in B group was selected randomly for MSCs or MNCs
transplantation as MSCs or MNCs group, the other lower limb in the same patient was selected
for placebo(normal saline ,NS)injection as NS group.
The whole procedures of this clinical trial were blinded to both patients and
investigators.Patients in both groups received the same ordinary treatment. Meanwhile, MSCs
and MNCs were transplanted into the impaired lower limbs respectively. Follow-up index
include: efficacy (pain,ulcer healing rate, lower limb amputation rate and ,ankle-brachial
index,Transcutaneous oxygen pressure,magnetic resonance angiography) and safety (infection
of the injection site, immunological rejection, and tumour generation).
RESEARCH DESIGN AND METHODS Written informed consent was obtained from all subjects. Type 2
diabetic patients with bilateral critical limb ischemia (ankle-brachial index, ABI from 0.30
to 0.60) and at least with one foot ulcer, but without malignant tumor or gangrene above the
ankle and/or severe coronary, cerebral and renal vascular disease, were eligible for the
participation in this trial. Eligible patients took part in this study on a voluntary basis.
They were randomized into the A and B group by use of a randomization table. One lower limb
in A group or in B group was selected randomly for BMMSCs or BMMNCs transplantation as
BMMSCs or BMMNCs group, the other lower limb in the same patient was selected for
placebo(normal saline ,NS)injection as NS group. The whole procedures of this clinical trial
were blinded to both patients and investigators.
Preparation of Human Autologous Serum Preparation of MSCs and MNCs Flow Cytometric Analysis
Examination of cells Safety Administration of therapy 5.0*108~5.0*109 MSCs and MNCs were
transplant into impaired lower limbs by intramuscular injection.
observation index and assessment guidelines Statistical analysis
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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