National Collaborative Centre for Hepatic Regenerative Medicine (NC-CHRM): Single vs Repeated Cycle of Granulocyte Colony-Stimulating Factor (GCSF) & Darbepoetin in Early Decompensated Cirrhosis
NCT ID: NCT07131280
Last Updated: 2025-08-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
110 participants
INTERVENTIONAL
2025-09-30
2031-12-31
Brief Summary
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Detailed Description
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Novelty: Cirrhosis as a result of hepatitis B and C can regress with effective antiviral therapy. Therapeutic options for patients with cryptogenic or alcoholic cirrhosis are, however, limited. With limited options for transplant. Liver failure is failure of regeneration hence, potentiating native liver repair and regeneration can serve as potential non-transplant approaches. Growth factors {like GCSF, darbepoetin (EPO) have shown survival benefits with improve liver repair and regeneration in clinical trials by us (Gastroenterology 2012, 2015, Liver Int. 2019; Hepatology 2021) and others, however the effect is transient. In the proposed National Collaborative Centre for Hepatic Regenerative Medicine (NC-CHRM) we will use this novel regenerative medicine approaches GCSF therapy (for management of chronic liver failure) to develop safe and effective regenerative therapy clinical protocol for transplant free management of liver failure in cirrhosis. Using integrated cellular, molecular and functional analysis we will also establish their mechanism of action and identify biomarker to access therapeutic response.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Three cycles of GCSF+ darbepoetin and standard medical treatment
Patient randomize for Three cycle of GCSF+ darbepoetin together with standard medical treatment, G-CSF will be given at a dose of 5 μg/kg s/c at days 1, 2, 3, 4, 5 and then every third and 7th day till day 30 based on hematological response and darbepoetin will be given s/c at dose of 40mcg once a week (total 4 doses) for 1 month. Second cycle of GCSF+ darbepoetin will be given after 1 month of completion of first cycle that is at month 3 and third cycle will be given 1 month after completion of 2nd cycle that is at 5th month. All patients will receive the standard medical treatment.
Gcsf
G-CSF will be given at a dose of 5 μg/kg s/c at days 1, 2, 3, 4, 5 and then every third and 7th day till day 30
Darbepoetin
Darbepoetin will be given s/c at dose of 40mcg once a week for 1 month
Standard Medical Treatment
Standard Medical Treatment
Single cycle of GCSF+ darbepoetin and standard medical treatment
Patient randomize for Single cycle of GCSF+ darbepoetin together with standard medical treatment, G-CSF will be given at a dose of 5 μg/kg s/c at days 1, 2, 3, 4, 5 and then every third and 7th day till day 30 based on hematological response and darbepoetin will be given s/c at dose of 40mcg once a week (total 4 doses) for 1 month. All patients will receive the standard medical treatment.
Gcsf
G-CSF will be given at a dose of 5 μg/kg s/c at days 1, 2, 3, 4, 5 and then every third and 7th day till day 30
Darbepoetin
Darbepoetin will be given s/c at dose of 40mcg once a week for 1 month
Standard Medical Treatment
Standard Medical Treatment
Interventions
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Gcsf
G-CSF will be given at a dose of 5 μg/kg s/c at days 1, 2, 3, 4, 5 and then every third and 7th day till day 30
Darbepoetin
Darbepoetin will be given s/c at dose of 40mcg once a week for 1 month
Standard Medical Treatment
Standard Medical Treatment
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients with Grade III ascites
* CHILD C cirrhosis
* Patients with a known focus of sepsis; spontaneous Bacterial Peritonitis (SBP)
* variceal bleeding in past 3months
* Hepatocellular Carcinoma (HCC) or other malignancy
* Acute Kidney Injury (AKI) with serum Creatinine \>1.5 mg/ dl, multi-organ failure, grade 3 or 4 Hepatic Encephalopathy (HE),
* HIV seropositivity
* Medically uncontrolled essential hypertension
* Pregnancy
* Viral etiology of liver disease
* Co-existent Hepatitis B, Hepatitis C, HIV
* Chronic kidney disease
* Lack of informed consent
18 Years
65 Years
ALL
No
Sponsors
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Indian Council of Medical Research
OTHER_GOV
Institute of Liver and Biliary Sciences, India
OTHER
Responsible Party
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Principal Investigators
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Dr. Shiv Kumar Sarin, DM
Role: PRINCIPAL_INVESTIGATOR
Institute of Liver & Biliary Sciences
Locations
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Institute of Liver & Biliary Sciences
New Delhi, , India
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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ILBS-Cirrhosis-75
Identifier Type: -
Identifier Source: org_study_id
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