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Effect of Granulocyte colony stimulating factor (G-CSF) on survival of children with Acute on Chronic Liver Failure

Role of Granulocyte colony stimulating factor (G-CSF) on short term outcome of children with acute on chronic liver failure in a non-transplant unit

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010420
Enrollment
40
Registered
2017-11-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Children diagnosed with Acute on Chronic Liver Failure, presenting with or without Hepatic Encephalopathy Grade 1 or Grade 2

Interventions

Intervention1: No GCSF: Comparison of GCSF and no GCSF in study group and control group of children with Acute on chronic Liver Failure Control Intervention1: Granulocyte colony stimulating factor (G-

Sponsors

Departmental Fund
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Jaundice and coagulopathy, complicated within 4 weeks by ascites and/or encephalopathy. 2. Evidence of chronic liver disease on history/examination/investigations 3. Jaundice [serum bilirubin >5 mg/dl] 4. Coagulopathy (INR >1.5/prothrombin activity 5. Complicated within 4 weeks by ascites and/or encephalopathy (as determined by clinical examination).

Exclusion criteria

Exclusion criteria: 1. Previous episodes of Decompensated cirrhosis 2. Tropical infection related hepatopathy with high grade fever 3. Age of 4. Portal vein thrombosis 5. Severe sepsis/ Multi-organ failure at presentation 6. Grade 3 or 4 hepatic encephalopathy 7. HIV seropositive 8. Any previous known hypersensitivity to G-CSF 9. Any significant comorbidity 10. Refusal to participate in the study

Design outcomes

Primary

MeasureTime frame
To compare the outcome of children with ACLF receiving GCSF with those not receiving GCSF at Day 30 and Day 60Timepoint: To compare the outcome of children with ACLF receiving GCSF with those not receiving GCSF at Day 30 and Day 60

Secondary

MeasureTime frame
CD 34 cell count Clinical and Biochemical ProfileTimepoint: 60 days

Countries

India

Contacts

Public ContactShruti Sharma

PGIMER

sadhnalal2014@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 1, 2026