Skip to content

Bone Marrow Autograft in Limb Ischemia

Cell Therapy in Critical Limb Ischemia

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00904501
Acronym
BALI
Enrollment
40
Registered
2009-05-19
Start date
2009-03-31
Completion date
2015-01-31
Last updated
2016-03-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peripheral Vascular Diseases

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

Etablissement Français du Sang
CollaboratorOTHER
CHU de Reims
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frame
Major amputation rate and mortality6 months

Secondary

MeasureTime frame
Clinical symptoms and haemodynamical parameters6 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026