Human Umbilical Cord Mesenchymal Stem Cell Transplantation for The Treatment of Acute-on-Chronic Liver Failure
Condition(s) studied
Investigational drug(s) / intervention(s)
standard medical treatment: standard medical treatment for ACLF
Placebo: 5% human serum albumin in 0.9% saline (at week0, week1 and week2)
hUC-MSC: hUC-MSC (1.5×10\^8 cells/time, Peripheral IV, at week0, week1 and week2)
hUC-MSC_Prolonged: hUC-MSC (1.5×10\^8 cells/time, Peripheral IV, at week4 and week5)
Study summary
This study is a randomized double-blind placebo-controlled multicenter clinical trial to evaluate the safety and efficacy of human umbilical cord mesenchymal stem cell (UC-MSC) transplantation for the treatment of acute-on-chronic liver failure (ACLF). UC-MSC therapy may improve the clinical outcomes of patients with ACLF. The trial would provide scientific evidence for UC-MSC transplantation as a potential treatment for ACLF.
Eligibility
Primary outcome measure(s)
- Transplantation free survival rate — week1, week2, week3, week4, week5, week8, week12, week24, week53
Transplantation free survival rate of ACLF patients. - Incidence of Treatment-Emergent Adverse Events — day0, day3, week1, week2, week3, week4, week5, week8, week12, week24, week53
Safety and Tolerability of UC-MSCs transplantation.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| the Fifth Medical Center, Chinese PLA General Hospital | Beijing | Beijing Municipality | Recruiting |
More Beijing 302 Hospital trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05985863 on ClinicalTrials.gov ↗ ← All trials in China