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Allogenic UCMSCs as Adjuvant Therapy for Severe COVID-19 Patients — UCMSC  

Covid 19 Clinical Trial

Official title:
Efficacy and Safety of Normoxic Allogenic Umbilical Cord Mesenchymal Stem Cells Administered as Adjuntive Treatment to Standard Treatment in Severe Patients With COVID-19

Clinical Trial Summary

This study is conducted to assess the efficacy and safety of stem cells as adjunctive treatment for severe COVID-19 patients. Here, we want to study whether the administration of mesenchymal stem cells are safe and able to relieve some of the COVID-19 symptoms

Clinical Trial Description

This is a randomized controlled trial. double-blind, multi-center clinical study conducted at three different hospitals, on 21 patients who received intervention and 21 patients who received control treatment. The purpose of this study is to evaluate the efficacy and safety of intravenous administration of normoxic allogeneic umbilical cord-derived mesenchymal stem cell (UCMSC) in the treatment group, compared to the control group who are only given standard COVID-19 treatments and normal saline infusion ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05132972
Study type Interventional
Source Kementerian Riset dan Teknologi / Badan Riset dan Inovasi Nasional, Indonesia
Contact Bintang Soetjahjo, MD PhD
Phone +628122987359
Email bjortho@yahoo.com
Status Recruiting
Phase Phase 2/Phase 3
Start date January 17, 2021
Completion date November 2021
View Details
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