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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01663376
Other study ID # KSC-MSCs-CLI
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2009
Est. completion date April 2011

Study information

Verified date June 2019
Source R-Bio
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate the efficacy and safety of autologous transplantation of Adipose Tissue derived Mesenchymal stem cells (MSCs) in patient with critical limb ischemia


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 2011
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- At least 6 months since the onset CLI(Chronic ASO or Buerger disease)

- Patients with luminal stenosis > 50% by leg angiography

- Age is between 20 and 80

- Patients whose Rutherford's class is II-4, III-5 or III-6 (Patients with rest pain or ischemic ulcer/necrosis)

- Patients for whom angioplasty and bypass surgery are not indicated because of anatomical or procedural reasons or frequent reocclusion/restenosis following traditional revascularization

- Patients who can give informed consent themselves in writing

Exclusion Criteria:

- Previous or current history of neoplasm or comorbidity that could impact the patient's survival

- Detection of proximal source of emboli including atrial fibrillation

- Primary hematologic disease, including hypercoagulable states

- Detection of proliferative retinopathy

- Entrapment syndrome

- Alcohol abuse, cocaine amphetamine etc.

- Detection of osteomyelitis

- Uncontrolled DM

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Autologous Adipose Tissue derived MSCs Transplantation
Intramuscular injection of Autologous Adipose Derived Mesenchymal Stem Cells. Dose : 1x10e8 ~3x10e8 cells

Locations

Country Name City State
Korea, Republic of Pusan National University Hospital Pusan

Sponsors (2)

Lead Sponsor Collaborator
R-Bio Pusan National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Lee HC, An SG, Lee HW, Park JS, Cha KS, Hong TJ, Park JH, Lee SY, Kim SP, Kim YD, Chung SW, Bae YC, Shin YB, Kim JI, Jung JS. Safety and effect of adipose tissue-derived stem cell implantation in patients with critical limb ischemia: a pilot study. Circ J — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Major Adverse Events Analysis (MAEs) To evaluate the change of treated critical limb ischemia before cell implantation and at 3, 6, 12 months post injection of MSCs 48 weeks
Secondary Ankle-Brachial Index (ABI) To evaluate the change of treated critical limb ischemia before cell implantation and at 3, 6, 12 months post injection of MSCs. 48 weeks
Secondary Digital subtraction angiography (DSA) To evaluate the change of treated critical limb ischemia before cell implantation and at 3, 6, 12 months post injection of MSCs. 48 weeks
Secondary Thermography To evaluate the change of treated critical limb ischemia before cell implantation and at 3, 6, 12 months post injection of MSCs. 48 weeks
Secondary Wong-Baker FACES Pain Rating Score To evaluate the change of treated critical limb ischemia before cell implantation and at 3, 6, 12 months post injection of MSCs. 48 weeks
Secondary Treadmill test To evaluate the change of treated critical limb ischemia before cell implantation and at 3, 6, 12 months post injection of MSCs. 48 weeks
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