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Cell Therapy With Bone Marrow Mononuclear Cells in Critical Leg Ischemia (CLI)

Optimisation d'un Produit de thérapie Cellulaire Autologue Par Cellules mononucléées médullaires Dans l'ischémie Critique Des Membres inférieurs liée à l'athérosclérose

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00377897
Enrollment
20
Registered
2006-09-19
Start date
2005-01-31
Completion date
2009-12-31
Last updated
2009-02-16

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

Conditions

Critical Leg Ischemia

Keywords

critical leg ischemia, PAD, cell therapy

Brief summary

This study will treat by cell therapy 20 patients with critical leg ischemia (CLI) not eligible for revascularization or angioplasty. It will use exactly the same protocol as published by Tateishi-Yuyama et al. (Lancet 2002), using bone-marrow mononuclear cells (BMMNC).

Detailed description

Patients will be included with CLI according to the TASC criteria. Under general anesthesia, 500 ml of bone marrow is harvested in both iliac crests. After isolation and concentration of the BMMNC in 30 ml, 40 injections of around 0.75 ml will be done in the gastrocnemius of the ischemic leg, within 3 hours after preparation of the cell therapy product. Patients will then be followed-up every week during one month and then every month during one year. This study was approved by the ethical committee of Paris-Broussais HEGP (France) and our french regulatory agency (AFSSAPS). It began including patients in January 2005 and will last until December 2007.

Interventions

PROCEDUREcell therapy

Injection of Bone-Marrow mononuclear cells in the muscles of the calf.

Sponsors

Assistance Publique - Hôpitaux de Paris
CollaboratorOTHER
University of Paris 5 - Rene Descartes
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Age \> 18 * Signature of informed consent * Critical leg ischemia with ankle pressure \< 70 mmHg * Ischemic ulcer or gangrene * No possibility of surgical revascularization * No possibility of angioplasty

Exclusion criteria

* Cancer * Suspicion of a cancer on X-Ray, mammography or elevated PSA * Age \< 18 * Life expectancy \< 6 months * Active retinopathy * Angioplasty or surgical revascularization within 3 months * Stoke within 3 months * HIV + or HCV/HBC+

Design outcomes

Primary

MeasureTime frame
Ankle brachial index6 months
Healing1 year
Amputation rate1 year

Secondary

MeasureTime frame
TcPO26 months

Countries

France

Contacts

Primary ContactJoseph Emmerich, MD, PhD
joseph.emmerich@egp.aphp.fr33 1 56 09 30 51
Backup ContactSaliha Djane, MD
saliha.djane@sls.aphp.fr33 1 44 84 17 45

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026