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Clinical Trial Summary

This study is designed to evaluate the efficacy, safety and tolerability of autologous bone marrow derived mesenchymal stem cells compared to placebo (sham operation) when administered via percutaneous coronary infusion to patients with ischemic heart disease, who are screened by D-SPECT and have pretreated with 3-month cardiac shock wave therapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03397095
Study type Interventional
Source Shanghai 10th People's Hospital
Contact Yuxi Sun
Phone +86 15216718171
Email zhggsmlsyx@163.com
Status Recruiting
Phase Phase 1/Phase 2
Start date April 3, 2018
Completion date April 1, 2022

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