Could stem cells offer a lifeline for End-Stage liver disease?
NCT ID NCT06167473
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether umbilical cord stem cells given through a vein could help people with end-stage liver disease. Twenty-two adults received different doses to see if it improved survival and liver function. The goal was to find a safer, more accessible alternative to liver transplants.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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22 people
The number who actually took part.
- Started
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Nov 2023
- 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
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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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. Sign 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
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General Hospital of Northern Theater Command
Shenyang, Liaoning, 110840, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.