Skip to content

Intramuscular Mononuclear Cells and Mesenchymal Stem Cells Transplantation to Treat Chronic Critical Limb Ischemia

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

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01456819
Enrollment
50
Registered
2011-10-21
Start date
2011-03-31
Completion date
2016-02-29
Last updated
2015-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critical Limb Ischemia

Keywords

autologous, bone marrow, critical limb ischemia, efficacy, mesenchymal stem cells, mononuclear cells

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.

Interventions

BIOLOGICALMononuclear and mesenchymal stem cells

Intramuscular administration into the ischemic limb

Intramuscular administration into the ischemic limb

Sponsors

Cytopeutics Sdn. Bhd.
CollaboratorINDUSTRY
National University of Malaysia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in angiogenesis1 month, 3 months, 6 months, 9 months, 12 monthsMeasurement of angiogenesis by presence of peripheral pulses, capillary refill and transcutaneous oxygen saturation (TCOS).

Secondary

MeasureTime frameDescription
Change in ulcer size1 month, 3 months, 6 months, 9 months, 12 monthsMeasurement of ulcer size by clinical assessment and grid maps.
Visual Analog Score1 month, 3 months, 6 months, 9 months, 12 months
Exercise Treadmill Test1 month, 3 months, 6 months, 9 months, 12 months
Improvement in vascularity and blood supply1 month, 3 months, 6 months, 9 months and 12 monthsMeasured by digital subtraction angiography (DSA) and ankle brachial systemic pressure index (ABI).

Countries

Malaysia

Contacts

Primary ContactHanafiah Harunarashid, MD
hanafiah@ppukm.ukm.my+60391456208

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026