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Combination Stem Cell Therapy for the Treatment of Severe Leg Ischemia (mesendo)

Primary Purpose

Critical Limb Ischemia, Peripheral Vascular Disease

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Mesendo
Sponsored by
TCA Cellular Therapy
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Limb Ischemia focused on measuring A hypoperfusion of the blood through a leg, Stem cells, Stem cell transplantation, Stem cell autologous transplantation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Males or females older than 18 years of age.
  • Limb ischemia with ABI of £ 0.6 in the index lower extremity in two consecutive examinations done at least 1 week apart.
  • Limb ischemia with resting ischemic pain and/or non-healing ulcers.
  • Patients not considered candidates for surgical or percutaneous revascularization, due to poor target vessels, inability to cross total occlusions, or a morbidity which precludes general anesthesia

Exclusion Criteria:

  • Inability to provide informed consent.
  • Previous angiogenic therapy.
  • Known sensitivity to gentamycin and/or amphotericin B.
  • Use or expected use of antineoplastic drugs.
  • Any illness which might affect the patient's survival after enrollment in the protocol.
  • Any illness or significant laboratory abnormality, which in the investigator's judgment will interfere with the patient's ability to comply with the protocol, compromise the patient's safety, or interfere with the interpretation of the study results.
  • No evidence of acute infection - WBC > 15000.
  • WBC < 4000.
  • Serum Creatinine > 3.0 mg/dL.
  • Pregnant women or women planning to become pregnant.
  • Recent myocardial infarction within 3 months prior to screening.

Sites / Locations

  • TCA Cellular Therapy

Outcomes

Primary Outcome Measures

Safety

Secondary Outcome Measures

Full Information

First Posted
August 16, 2007
Last Updated
April 27, 2011
Sponsor
TCA Cellular Therapy
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1. Study Identification

Unique Protocol Identification Number
NCT00518401
Brief Title
Combination Stem Cell Therapy for the Treatment of Severe Leg Ischemia
Acronym
mesendo
Official Title
Phase I Study of A Combination Stem Cell Therapy is Safe and Feasible in the Development of Mature Stable Vessels in Ischemic Limbs
Study Type
Interventional

2. Study Status

Record Verification Date
February 2010
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
October 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
TCA Cellular Therapy

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research study is to determine if the transplant of a combination of stem cells obtained from the bone marrow of the same patient will contribute to the formation of new blood vessels in the severely diseased ischemic limb (leg). In this study the safe use of this combination of stem cells and its effects on making new blood vessels will be evaluated. Limb Ischemia (LI) is a severe obstruction of the arteries which seriously decreases blood flow to the extremities (mainly feet and legs) and has progressed to the point of severe pain and even skin ulcers or sores. LI needs comprehensive treatment since the condition will not improve on its own. The overall goal of treatment is to reduce the pain and increase blood flow to improve symptoms or save the leg or feet. In many cases, current options for treatment including medications, surgery or endovascular procedures have not been successful. In the last few years, investigators have explored therapies aimed to increase blood flow to the ischemic vessels by transplanting cells that will promote the development of new vessels in the diseased leg. The study hypothesis is based on the concept that the process of formation of new blood vessels is complex and requires the participation of several types of stem cells and growth factors. The lack of any of these components will produce vessels which are immature and unable to provide appropriate blood supply to the leg. Patients eligible to participate in this study are those suffering from poor circulation or severe leg blockages, which are not candidates for surgical procedures. Once the mixture of stem cells is prepared and the patient's bone marrow is ready, cells will be transplanted into the calf muscle of the diseased leg. Clinical studies to evaluate if the transplant works and is safe will be performed up to 1 year after cell transplant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Limb Ischemia, Peripheral Vascular Disease
Keywords
A hypoperfusion of the blood through a leg, Stem cells, Stem cell transplantation, Stem cell autologous transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Mesendo
Intervention Description
Intramuscular injection of 0.5 cc per site of the combination stem cell mixture in approximately 40 different ischemic sites of the gastrocnemius area of the calf.
Primary Outcome Measure Information:
Title
Safety
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males or females older than 18 years of age. Limb ischemia with ABI of £ 0.6 in the index lower extremity in two consecutive examinations done at least 1 week apart. Limb ischemia with resting ischemic pain and/or non-healing ulcers. Patients not considered candidates for surgical or percutaneous revascularization, due to poor target vessels, inability to cross total occlusions, or a morbidity which precludes general anesthesia Exclusion Criteria: Inability to provide informed consent. Previous angiogenic therapy. Known sensitivity to gentamycin and/or amphotericin B. Use or expected use of antineoplastic drugs. Any illness which might affect the patient's survival after enrollment in the protocol. Any illness or significant laboratory abnormality, which in the investigator's judgment will interfere with the patient's ability to comply with the protocol, compromise the patient's safety, or interfere with the interpretation of the study results. No evidence of acute infection - WBC > 15000. WBC < 4000. Serum Creatinine > 3.0 mg/dL. Pregnant women or women planning to become pregnant. Recent myocardial infarction within 3 months prior to screening.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gabriel P. Lasala, MD, FACC
Organizational Affiliation
TCA Cellular Therapy
Official's Role
Principal Investigator
Facility Information:
Facility Name
TCA Cellular Therapy
City
Covington
State/Province
Louisiana
ZIP/Postal Code
70433
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Combination Stem Cell Therapy for the Treatment of Severe Leg Ischemia

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