Intramuscular Mononuclear Cells and Mesenchymal Stem Cells Transplantation to Treat Chronic Critical Limb Ischemia
Primary Purpose
Critical Limb Ischemia
Status
Unknown status
Phase
Phase 2
Locations
Malaysia
Study Type
Interventional
Intervention
Mononuclear and mesenchymal stem cells
Mononuclear cells
Sponsored by

About this trial
This is an interventional treatment trial for Critical Limb Ischemia focused on measuring autologous, bone marrow, critical limb ischemia, efficacy, mesenchymal stem cells, mononuclear cells
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of critical limb ischemia leading to ischemic ulcers in which amputation is indicated
- Not suitable for, or remain symptomatic despite angioplasty, bypass operation or collateralization
Exclusion Criteria:
- Contraindication to epidural anesthesia and bone marrow aspiration
- Contraindication to contrast angiography
- Evidence of neoplasia and bone marrow diseases
- Any acute or chronic communicable diseases including Hepatitis B, Hepatitis C and HIV
- Patients with a limited life expectancy (< 1 year)
- Patients with myocardial infarction or stroke within 6 months
- Patients with coronary intervention within 6 months
- Renal impairment indicated by serum creatinine greater than two times upper limit of the normal range
- Liver impairment indicated by serum aspartate transaminase and alanine transaminase greater than two times upper limit of normal
- Any other co-morbidity which the physician deems as a contraindication to stem cell transplantation
Sites / Locations
- UKM Medical CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Mononuclear and mesenchymal stem cells
Mononuclear cells only
Arm Description
Autologous bone marrow-derived mononuclear cells and mesenchymal stem cells
Autologous bone marrow-derived mononuclear cells
Outcomes
Primary Outcome Measures
Change in angiogenesis
Measurement of angiogenesis by presence of peripheral pulses, capillary refill and transcutaneous oxygen saturation (TCOS).
Secondary Outcome Measures
Change in ulcer size
Measurement of ulcer size by clinical assessment and grid maps.
Visual Analog Score
Exercise Treadmill Test
Improvement in vascularity and blood supply
Measured by digital subtraction angiography (DSA) and ankle brachial systemic pressure index (ABI).
Full Information
NCT ID
NCT01456819
First Posted
October 4, 2011
Last Updated
April 9, 2015
Sponsor
National University of Malaysia
Collaborators
Cytopeutics Sdn. Bhd.
1. Study Identification
Unique Protocol Identification Number
NCT01456819
Brief Title
Intramuscular Mononuclear Cells and Mesenchymal Stem Cells Transplantation to Treat Chronic Critical Limb Ischemia
Official Title
Phase II Efficacy Study of Intramuscular Autologous Bone Marrow Mononuclear Cells Plus Mesenchymal Stem Cell Implantation Versus Autologous Bone Marrow Mononuclear Cells Implantation Only in Patients With Chronic Critical Limb Ischemia
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Unknown status
Study Start Date
March 2011 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
February 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National University of Malaysia
Collaborators
Cytopeutics Sdn. Bhd.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomized and single blinded study aimed to compare the efficacy between intramuscular autologous bone marrow mononuclear cells plus mesenchymal stem cell implantation and intramuscular autologous bone marrow mononuclear cells implantation only in patients with chronic critical limb ischemia. Patients will be randomized into two groups of equal number; patients in one group will be implanted with mononuclear cells and mesenchymal stem cells, and the other implanted with mononuclear cells only in the area of affected limb.
Detailed Description
When the long blood vessels supplying blood to the arms and legs become blocked (ischemic), patient will experience painful sensations in their calves when they walked which slowly become excruciating painful at rest. When the condition worsens, the patients will not be able to feel any pain from their legs and they will not know if there are any small ulcers or cuts on their legs. As a result, a small ulcer which goes unnoticed becomes bigger and can sometimes become infected. In the worst situations, infection might lead towards gangrene and septicaemia. Severe rest pain and/or ulcerations of ischemic limbs are defined as the state of chronic critical limb ischemia and at this point, amputation of the affected limb is suggested.
Conventional treatments include angioplasty/bypass operation to remove blood vessel blockage to restore blood supply, the use of prescribed medicines to aid in ulcer recovery and clear infection and debridement of damaged/infected tissue. Some procedures have to be performed multiple times. Amputation is inevitable in many cases because some blood capillaries cannot be corrected and restenosis of vessels is very common. Cell therapy with mononuclear cells and mesenchymal stem cells from bone marrow is promising because these stem cells are capable of stimulating and regenerating capillaries and blood vessels.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Limb Ischemia
Keywords
autologous, bone marrow, critical limb ischemia, efficacy, mesenchymal stem cells, mononuclear cells
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Mononuclear and mesenchymal stem cells
Arm Type
Experimental
Arm Description
Autologous bone marrow-derived mononuclear cells and mesenchymal stem cells
Arm Title
Mononuclear cells only
Arm Type
Active Comparator
Arm Description
Autologous bone marrow-derived mononuclear cells
Intervention Type
Biological
Intervention Name(s)
Mononuclear and mesenchymal stem cells
Other Intervention Name(s)
BM-MNC and BM-MSC
Intervention Description
Intramuscular administration into the ischemic limb
Intervention Type
Biological
Intervention Name(s)
Mononuclear cells
Other Intervention Name(s)
BM-MNC
Intervention Description
Intramuscular administration into the ischemic limb
Primary Outcome Measure Information:
Title
Change in angiogenesis
Description
Measurement of angiogenesis by presence of peripheral pulses, capillary refill and transcutaneous oxygen saturation (TCOS).
Time Frame
1 month, 3 months, 6 months, 9 months, 12 months
Secondary Outcome Measure Information:
Title
Change in ulcer size
Description
Measurement of ulcer size by clinical assessment and grid maps.
Time Frame
1 month, 3 months, 6 months, 9 months, 12 months
Title
Visual Analog Score
Time Frame
1 month, 3 months, 6 months, 9 months, 12 months
Title
Exercise Treadmill Test
Time Frame
1 month, 3 months, 6 months, 9 months, 12 months
Title
Improvement in vascularity and blood supply
Description
Measured by digital subtraction angiography (DSA) and ankle brachial systemic pressure index (ABI).
Time Frame
1 month, 3 months, 6 months, 9 months and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinical diagnosis of critical limb ischemia leading to ischemic ulcers in which amputation is indicated
Not suitable for, or remain symptomatic despite angioplasty, bypass operation or collateralization
Exclusion Criteria:
Contraindication to epidural anesthesia and bone marrow aspiration
Contraindication to contrast angiography
Evidence of neoplasia and bone marrow diseases
Any acute or chronic communicable diseases including Hepatitis B, Hepatitis C and HIV
Patients with a limited life expectancy (< 1 year)
Patients with myocardial infarction or stroke within 6 months
Patients with coronary intervention within 6 months
Renal impairment indicated by serum creatinine greater than two times upper limit of the normal range
Liver impairment indicated by serum aspartate transaminase and alanine transaminase greater than two times upper limit of normal
Any other co-morbidity which the physician deems as a contraindication to stem cell transplantation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hanafiah Harunarashid, MD
Phone
+60391456208
Email
hanafiah@ppukm.ukm.my
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hanafiah Harunarashid, MD
Organizational Affiliation
UKM Medical Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
UKM Medical Centre
City
Kuala Lumpur
ZIP/Postal Code
56000
Country
Malaysia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hanafiah Harunarashid, MD
First Name & Middle Initial & Last Name & Degree
Hanafiah Harunarashid, MD
First Name & Middle Initial & Last Name & Degree
Mohammad Azim Mohammad Idris, MD
12. IPD Sharing Statement
Learn more about this trial
Intramuscular Mononuclear Cells and Mesenchymal Stem Cells Transplantation to Treat Chronic Critical Limb Ischemia
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