Stem cells show promise for failing livers
NCT ID NCT06242405
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether multiple infusions of stem cells from donated umbilical cords could help people with end-stage liver disease. 92 adults received the stem cells through a vein, and researchers tracked liver function and complications. The goal was to see if repeated doses work better than a single dose.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- umbilical cord mesenchymal stem cells
- What this could lead to
- If successful, this could point toward a way to improve liver function and reduce complications in people with end-stage liver disease, potentially delaying the need for a transplant.
- What could go wrong
- This is a small, completed study with 92 participants and no control group, so results may not be conclusive. Stem cell infusions carry risks like infection or immune reactions, and the long-term benefits are uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
92 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 80 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 1\. 18-80 years old * 2\. End-stage liver disease * 3\. Signed informed consent Exclusion Criteria: * 1\. Tumours of the liver or other organs * 2\. Liver transplantation recipients * 3\. Acute myocardial infarction, acute heart failure, type I and type II respiratory failure, pulmonary embolism, acute cerebral infarction, acute cerebral haemorrhage and other serious cardiopulmonary diseases * 4\. Other diseases that may seriously affect the survival * 5\. Human immunodeficiency syndrome * 6\. Interferon or glucocorticoid therapy within 1 year * 7\. Treated for mental illness * 8\. Participation in other clinical trials within 30 days * 9\. Pregnant or breastfeeding subjects * 10\. Allergic asthma, allergic urticaria, eczema, or a history of multiple drug and food allergies * 11\. Other circumstances that are unsuitable for participation in this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
General Hospital of Northern Theater Command
Shenyang, Liaoning, 110840, China
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Other studies related to the condition(s) this trial covers.
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