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The Safety and Efficacy of Human Umbilical Cord Mesenchymal Stem Cells (19#iSCLife®-ACI) in the Treatment of Acute Cerebral Infarction

Cerebral Infarction Clinical Trial

Official title:
Study the Safety and Efficacy of Human Umbilical Cord-derived Mesenchymal Stem Cells in the Treatment of Acute Cerebral Infarction

Clinical Trial Summary

The purposes of the study is to determine the safety and efficacy of treating acute ischemic stroke patients with human umbilical cord mesenchymal stem cells (hUC-MSC).

Clinical Trial Description

This is a randomized, double-blind, paralleled study. 40 patients will be separated into two groups, and receive basic treatment (Aspirin Tablet). Patients in experimental group will receive hUC-MSC once a month, total 3 times. After the treatment, investigator will have follow-up visit for 6 months, evaluate the security and efficacy of hUC-MSC. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03186456
Study type Interventional
Source Sclnow Biotechnology Co., Ltd.
Contact
Status Suspended
Phase Phase 1
Start date December 31, 2024
Completion date December 31, 2025
View Details
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