Intra-arterial Stem Cell Therapy for Patients With Chronic Limb Ischemia (CLI) (JUVENTAS)

UMC Utrecht

Status and phase: Completed; Phase 2; Phase 1

Conditions: Peripheral Vascular Diseases; Arterial Occlusive Diseases; Ischemia; Gangrene; Leg Ulcer

Treatments: Procedure: BM-MNC infusion; Procedure: Bone marrow punction; Procedure: Placebo infusion

Study type: Interventional

Funder types: Other

Identifiers

NCT00371371

JUVENTAS

06/030 (Other Grant/Funding Number)

CS 06.007

Details and patient eligibility

About

The purposes of this study are to determine whether intra-arterial injection of autologous stem cells is effective in the treatment of chronic limb ischemia (CLI), to characterize stem cell dysfunction in patients with CLI, and to relate the stem cell function with clinical outcome.

Full description

Despite advances in surgical and radiological vascular techniques, a significant number of patients with chronic critical limb ischaemia (CLI) are not eligible for revascularization procedures, often leaving amputation as the only option. Consequently, exploring new strategies for revascularization of ischemic limbs is of major importance. Preclinical studies and pioneering clinical trials suggest that administration of bone marrow (BM) mononuclear cells (MNC) into ischemic limbs enhances neovascularization, improves tissue perfusion and prevents amputation. However, no definite proof is available as the clinical studies thus far have been small and lacked double-blinded controls.

JUVENTAS is a randomized, double-blinded placebo-controlled trial in 109 - 160 patients with CLI to investigate the potential clinical effects of repeated intra-arterial infusion of BM-MNC in these patients (the exact number of patients to be included cannot be specified in advance because of the planned group sequential interim analyses). In addition, it will study the functional characteristics of the BM-MNC obtained from CLI patients and relate BM-MNC dysfunction to clinical outcome.

Enrollment: 160 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age > 18 years
• Severe infra-popliteal peripheral arterial occlusive disease [PAOD] (Fontaine class IIb, III or IV)
• Invalidating intermittent claudication, persistent, recurring rest pain requiring analgesia and/or non-healing ulcers present for > 4 weeks without evidence of improvement in response to conventional therapies
• Ankle brachial index < 0.6 or "unreliable"
• Not eligible for surgical or radiological revascularization
• Written informed consent

Exclusion criteria

• History of neoplasm or malignancy in the past 10 years
• Serious known concomitant disease with life expectancy of less than one year
• Anticipated inability to obtain 100 ml of bone marrow aspirate
• Known infection with human immunodeficiency virus (HIV), hepatitis B or hepatitis C virus
• Follow-up impossible

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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160 participants in 2 patient groups, including a placebo group

BM-MNC

Experimental group

Description:

autologous bone marrow-derived mononuclear cells

Treatment:

Procedure: Bone marrow punction

Procedure: BM-MNC infusion

Placebo

Placebo Comparator group

Description:

Placebo

Treatment:

Procedure: Placebo infusion

Procedure: Bone marrow punction