Allogeneic Mesenchymal Stem Cells for the Critical Limb Ischemia Therapy
Primary Purpose
Critical Limb Ischemia
Status
Unknown status
Phase
Phase 1
Locations
Russian Federation
Study Type
Interventional
Intervention
Mesenchymal stem cells
Normal saline
Sponsored by

About this trial
This is an interventional treatment trial for Critical Limb Ischemia
Eligibility Criteria
Inclusion Criteria:
- Males or females in the age group of 18-80 yrs of Caucasian origin.
- Peripheral artery disease (PAD) against the background of atherosclerosis and diabetes mellitus (DM)
- Critical lower limb ischemia (stages 3-4 by Fontaine-Pokrovsky or stages 4-6 by Rutherford)
- Patients with remaining symptoms of critical limb ischemia (CLI) in spite of the performed surgical (endovascular or open) treatment and continuing conservative therapy
- Patients with absent emergency indications to major amputation
- Patients planned for the reconstructive surgery with a questionable remote outcome due to compromised blood outflow
- Ankle Brachial Pressure Index (ABPI) ≤ 0.5 or ankle pressure ≤ 70 mm Hg
- Patients, if having associated Type II Diabetes, should be on medication and well controlled (HbA1c ≤ 8.5 %)
- On regular medication for hypertension if needed
- Normal liver and renal function (or having clinically insignificant deviations, according to the treating physician's opinion)
- Patients who are able to understand the requirements of the study, and willing to provide voluntary written informed consent, abide by the study requirements, and agree to return for required follow-up visits
Exclusion Criteria:
- Humid gangrene or acute/chronic infection of lower limb.
- Dry gangrene with extensive foot lesion (> 1\2).
- Acute arterial failure.
- Life-threatening conditions and predicted life expectancy of < 6 months.
- Presence of neoplasm or bone marrow disease
- Signs of active or chronic, including latent, haemorrhage
- Any acute or chronic infectious disease
- Renal failure determined as twofold or higher elevation of serum creatinine as compared to the upper normal limit
- Hepatic failure determined as the bilirubin, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels elevated by two and more times over the upper normal limits
- Thrombocytopenia (platelet counts < 50,000 /µl), leukocytopenia (WBC < 4,000/µl), immunosuppressive therapy
- Pronounced neurological deficit
- Patients with gait disturbance for reasons other than CLI
- Patients not suitable for cell therapy, by the treating physician's opinion
- CLI patients requiring amputation at the proximal to the trans-metatarsal level
- Patients with Type I diabetes
- Patients having respiratory complications/left ventricular ejection fraction < 25%
- Stroke or myocardial infarction within last 3 months
- Patients who are contraindicated for X-ray angiography
- History of severe alcohol or drug abuse within 3 months of screening
- Pregnant and lactating women.
- Patients tested positive for HIV 1, hepatitis C virus (HCV), hepatitis B virus (HBV)
- Unsigned informed consent
Sites / Locations
- Federal Research Clinical Center of Federal Medical & Biological AgencyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Mesenchymal stem cells
Normal saline
Arm Description
Mesenchymal stem cells, Intramuscular injection
Normal saline, Intramuscular injection
Outcomes
Primary Outcome Measures
Adverse events
Number of adverse events reported
Amputation-free survival
Number of survived patients
Secondary Outcome Measures
Limb salvage from major amputation
Number of patients who avoided amputation
Relief of the rest pain
Rest pain will be measured using the rest pain scale
Improvement in healing trophic disorders
Assessment of the severity of trophic ulcers
Improvement in perfusion by the ankle-brachial index
Measurements of the ankle-brachial index
Improvement in perfusion by radioisotope scintigraphy
Radioisotope scintigraphy study
Improvement in total walking distance (TWD) using a standard treadmill test
Standard treadmill test
Full Information
NCT ID
NCT03239535
First Posted
July 20, 2017
Last Updated
August 1, 2017
Sponsor
Federal Research Clinical Center of Federal Medical & Biological Agency, Russia
1. Study Identification
Unique Protocol Identification Number
NCT03239535
Brief Title
Allogeneic Mesenchymal Stem Cells for the Critical Limb Ischemia Therapy
Official Title
Allogeneic Mesenchymal Stem Cells for the Critical Limb Ischemia Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
August 2017
Overall Recruitment Status
Unknown status
Study Start Date
October 1, 2013 (Actual)
Primary Completion Date
August 1, 2018 (Anticipated)
Study Completion Date
November 1, 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Federal Research Clinical Center of Federal Medical & Biological Agency, Russia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The clinical trial aims to study the safety and efficacy of adult allogeneic mesenchymal stem cells for the treatment of critical limb ischemia.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Limb Ischemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Mesenchymal stem cells
Arm Type
Experimental
Arm Description
Mesenchymal stem cells, Intramuscular injection
Arm Title
Normal saline
Arm Type
Placebo Comparator
Arm Description
Normal saline, Intramuscular injection
Intervention Type
Biological
Intervention Name(s)
Mesenchymal stem cells
Intervention Description
Intramuscular injection
Intervention Type
Biological
Intervention Name(s)
Normal saline
Intervention Description
Intramuscular injection
Primary Outcome Measure Information:
Title
Adverse events
Description
Number of adverse events reported
Time Frame
24 months
Title
Amputation-free survival
Description
Number of survived patients
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Limb salvage from major amputation
Description
Number of patients who avoided amputation
Time Frame
3, 6, 12, 24 months
Title
Relief of the rest pain
Description
Rest pain will be measured using the rest pain scale
Time Frame
Immediate, 3, 6, 12, 24 months
Title
Improvement in healing trophic disorders
Description
Assessment of the severity of trophic ulcers
Time Frame
Immediate, 3, 6, 12, 24 months
Title
Improvement in perfusion by the ankle-brachial index
Description
Measurements of the ankle-brachial index
Time Frame
Immediate, 3, 6, 12, 24 months
Title
Improvement in perfusion by radioisotope scintigraphy
Description
Radioisotope scintigraphy study
Time Frame
Immediate, 3, 6, 12, 24 months
Title
Improvement in total walking distance (TWD) using a standard treadmill test
Description
Standard treadmill test
Time Frame
Immediate, 3, 6, 12, 24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males or females in the age group of 18-80 yrs of Caucasian origin.
Peripheral artery disease (PAD) against the background of atherosclerosis and diabetes mellitus (DM)
Critical lower limb ischemia (stages 3-4 by Fontaine-Pokrovsky or stages 4-6 by Rutherford)
Patients with remaining symptoms of critical limb ischemia (CLI) in spite of the performed surgical (endovascular or open) treatment and continuing conservative therapy
Patients with absent emergency indications to major amputation
Patients planned for the reconstructive surgery with a questionable remote outcome due to compromised blood outflow
Ankle Brachial Pressure Index (ABPI) ≤ 0.5 or ankle pressure ≤ 70 mm Hg
Patients, if having associated Type II Diabetes, should be on medication and well controlled (HbA1c ≤ 8.5 %)
On regular medication for hypertension if needed
Normal liver and renal function (or having clinically insignificant deviations, according to the treating physician's opinion)
Patients who are able to understand the requirements of the study, and willing to provide voluntary written informed consent, abide by the study requirements, and agree to return for required follow-up visits
Exclusion Criteria:
Humid gangrene or acute/chronic infection of lower limb.
Dry gangrene with extensive foot lesion (> 1\2).
Acute arterial failure.
Life-threatening conditions and predicted life expectancy of < 6 months.
Presence of neoplasm or bone marrow disease
Signs of active or chronic, including latent, haemorrhage
Any acute or chronic infectious disease
Renal failure determined as twofold or higher elevation of serum creatinine as compared to the upper normal limit
Hepatic failure determined as the bilirubin, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels elevated by two and more times over the upper normal limits
Thrombocytopenia (platelet counts < 50,000 /µl), leukocytopenia (WBC < 4,000/µl), immunosuppressive therapy
Pronounced neurological deficit
Patients with gait disturbance for reasons other than CLI
Patients not suitable for cell therapy, by the treating physician's opinion
CLI patients requiring amputation at the proximal to the trans-metatarsal level
Patients with Type I diabetes
Patients having respiratory complications/left ventricular ejection fraction < 25%
Stroke or myocardial infarction within last 3 months
Patients who are contraindicated for X-ray angiography
History of severe alcohol or drug abuse within 3 months of screening
Pregnant and lactating women.
Patients tested positive for HIV 1, hepatitis C virus (HCV), hepatitis B virus (HBV)
Unsigned informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mikhail A Konoplyannikov, PhD
Phone
+79154027268
Email
mkonopl@mail.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vladimir P Baklaushev, MD, PhD
Organizational Affiliation
Deputy Director
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Pavel Yu Orekhov, MD, PhD
Organizational Affiliation
Vascular Surgeon
Official's Role
Principal Investigator
Facility Information:
Facility Name
Federal Research Clinical Center of Federal Medical & Biological Agency
City
Moscow
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mikhail A Konoplyannikov, PhD
Phone
+79154027268
Email
mkonopl@mail.ru
12. IPD Sharing Statement
Plan to Share IPD
No
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Allogeneic Mesenchymal Stem Cells for the Critical Limb Ischemia Therapy
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