Autologous Bone Marrow For Lower Extremity Ischemia Treating

Sponsor
Clinical Center of Cellular Technologies, Russia (Other)
Overall Status
Completed
CT.gov ID
NCT00753025
Collaborator
Samara State Medical University (Other), Regional hospital of Samara (Other)
42
3
16

Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether autologous bone marrow derived cells and isolated CD133+ fraction are effective in the treatment limb ischemia

Condition or Disease Intervention/Treatment Phase
  • Procedure: Bone marrow aspiration, injection of cells
  • Procedure: Bone marrow aspiration , injection of isolated CD 133+ cells
  • Procedure: Bone marrow aspiration, injection of saline
Phase 2

Detailed Description

The number of patients with low limb obliterating atherosclerosis steadily grows and compounds more than 20-25 % from all kinds of a cardiovascular pathology. At conservation of this tendency to 2020 the amputation percentage executed due to vessel diseases, can reach 45 %. Hemodynamics improvement in an extremity by surgery is possible at 40 - 70 % of patients even with the widespread and plural lesion of arteries, but results are not always satisfactory. The most actual is the problem of angiosurgical help to patients with distal forms of arterial occlusions, due to the difficulty or impossibility performing reconstructive interventions. In these cases the operations of an indirect revascularization referred on stimulation of a collateral blood flow are carried out. However, despite the reached successes, in some cases results of such interventions do not give desirable effect, search of new methods of treatment therefore is necessary. To date the most perspective methods of neoangiogenesis stimulation are a cellular therapy and gene-engineering technologies. Experimental researches on a model of local limb ischemia showed possibility of use of various cells for neoangiogenesis stimulation. A number of clinical researches at patients with obliterating limb diseases has shown efficacy of cellular therapy even at a critical ischemia. However randomized, the placebo-controlled researches based on principles of evidence based medicine while it is not enough for the convincing conclusions.

Study Design

Study Type:
Interventional
Actual Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Randomized Double Blind Placebo-Controlled Research Of Treatment Efficiency For Patients With Lower Extremity Arteriosclerosis Obliterans By Autologous Transplantation Of Bone Marrow Progenitor Cells
Study Start Date :
Oct 1, 2006
Actual Primary Completion Date :
Jun 1, 2007
Actual Study Completion Date :
Feb 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Experimental: CD133

Procedure: Bone marrow aspiration , injection of isolated CD 133+ cells
arm "CD133" receives injection of isolated CD 133+ cells

Experimental: TNC

Procedure: Bone marrow aspiration, injection of cells
Bone marrow is aspirated at patients in all arms. Arm "TNC" receives injection of total nucleated cells into ischemic muscle

Placebo Comparator: Placebo

Procedure: Bone marrow aspiration, injection of saline
arm "placebo" receives injection of saline

Outcome Measures

Primary Outcome Measures

  1. Increasing of painless walking distance [Within the first 30 days, 6 months and 12 months after injection]

Eligibility Criteria

Criteria

Ages Eligible for Study:
39 Years to 70 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • an obliterating lower extremity atherosclerosis IIB a stage (on Fontaine classification)

  • a painless walking distance of 10-50 m

  • pulse absence on аа. dorsalis pedis, tibialis posterior, poplitea

  • absence of a ischemia in a rest and necrotic changes

  • mainly distal form of disease (a lesion of a superficial femoral artery, a popliteal artery, anticnemion arteries) according to an angiography that testifies to impossibility of reconstructive operation performance

  • patients after a lumbar sympathectomy and a tibial bone osteoperforations executed previously

  • heavy smokers

Exclusion Criteria:
  • insulin depended diabetes

  • myocardial infarction or a stroke within last year

  • an idiopathic hypertensia III stage

  • anaemia and other diseases of blood

  • decompensation of the chronic diseases which are contraindications to any surgical operation

  • HIV infection

  • a virus hepatitis

  • oncologic diseases

  • chemotherapy in the anamnesis

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Clinical Center of Cellular Technologies, Russia
  • Samara State Medical University
  • Regional hospital of Samara

Investigators

  • Study Director: Olga Tyumina, PhD,

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00753025
Other Study ID Numbers:
  • CCCT001
First Posted:
Sep 16, 2008
Last Update Posted:
Sep 16, 2008
Last Verified:
Sep 1, 2008
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2008