Peripheral Vascular Diseases
Conditions
Keywords
Limb ischemia, Cell Therapy
Brief summary
BALI (Bone marrow Autograft in Limb Ischemia) is a randomized double-blind trial comparing implantation of bone marrow - mononuclear cells versus placebo in patients presenting with critical leg ischemia and no surgical option. The main end point is the survival without major amputation 6 months after implantation. Biological studies are performed on bone marrow mononuclear cells (BM-MNC) to evaluate their angiogenic properties.
Detailed description
One hundred and ten patients with critical leg ischemia and no surgical option will be included. A bone marrow harvest (500 mL under general anaesthesia) is performed and BM-MNC are separated and concentrated (30 mL) for all included patients. For half of them, the BM-MNC are implanted on the same day whereas the others are implanted with a placebo cell-product (30 mL saline with 4 ml peripheral blood). For these patients the BM-MNC are cryo-conserved. Only the cell therapy unit, neither the patient, nor the clinician, know whether BM-MNC or placebo is implanted. The main end point is the survival without major amputation 6 months after implantation. After this delay it is possible to use previously cryo-conserved BM-MNC. Likewise biological studies are performed on BM-MNC: flow-cytometry analysis of progenitor cells content, proteins and mRNAs expression, induced angiogenesis in animal models.
Interventions
Implantation of placebo
Sponsors
Study design
Eligibility
Inclusion criteria
* Critical limb ischemia * No possible surgical treatment
Exclusion criteria
* Ongoing infectious disease * Gangrene extending beyond the digits * Diabetes mellitus with HbA1c \> 7.5% or with proliferative retinopathy * History of malignant disease * Contra-indication to general anaesthesia * Chronic haemodialysis * Prothrombin Time \< 50% * Recent onset (within 3 months) of myocardial infarction or brain infarction * Contra-indication to modification of anti-platelet or anticoagulant therapy * History of heparin-induced thrombocytopenia * Unexplained haematological abnormality
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Major amputation rate and mortality | 6 months |
Secondary
| Measure | Time frame |
|---|---|
| Clinical symptoms and haemodynamical parameters | 6 months |
Countries
France