Could a growth hormone help people with End-Stage liver disease?
NCT ID NCT05253287
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether giving growth hormone to people with decompensated liver cirrhosis (advanced liver scarring) could improve their health and survival. The trial included 96 adults with this condition. Researchers measured how long patients survived without major complications or needing a liver transplant, and checked for side effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
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96 people
The number who actually took part.
- Started
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Feb 2022
- Finished
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Dec 2024
- 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. Age above 18 years. 2. Patients having confirmed diagnosis of decompensated cirrhosis, any etiology. 3. Patients having given an informed and written consent for participation in the study. Exclusion Criteria: 1. Acute on chronic liver failure. 2. Diagnosis of concomitant hepatocellular carcinoma or other active malignancy. 3. Severe cardiac dysfunction NYHA grade III/IV, Chronic obstructive pulmonary disease GOLD C or above. 4. Active alcohol abuse in last 3 months. 5. Known hypersensitivity to GH. 6. Human immunodeficiency virus seropositivity. 7. Patients on antiviral therapy for HCV, HBV or corticosteroid for autoimmune hepatitis those who have received it within the last 6 months. 8. TIPS insertion within 6 months prior to study inclusion. 9. Pregnancy \& lactation. 10. Uncontrolled diabetes (Hb A1c ≥ 9) or diabetic retinopathy. 11. Active sepsis.
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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
-
Postgraduate Institute of Medical education and Research
Chandigarh, Uttarakhand, 160012, India
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Other studies related to the condition(s) this trial covers.
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