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Clinical Trial Summary

This clinical trial to study the Safety and Efficacy of Autologous Mesenchymal stem cells in critical limb ischemia.


Clinical Trial Description

If the participant voluntarily agrees to participate in the clinical trial before registration, the investigator conducts a screening test to evaluate the participant's suitability.

A participant that satisfies all inclusion and exclusion criteria is assigned a test group(2-time injection group).

Participants conduct cell therapy within 30 days after bone marrow aspiration, and will re-inject autologous mesenchymal stem cells within 30 days after first injection.

Participants will make a total of 5 hospital visits after registration, and Safety and Efficacy will be evaluated based on a fixed procedure on every visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02477540
Study type Interventional
Source Pharmicell Co., Ltd.
Contact
Status Withdrawn
Phase Phase 1
Start date December 2019
Completion date June 2020

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