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A multi-center clinical study of granulocyte colony stimulating factor enhances survival in patients with liver failure and factors analysis that affect the therapeutic effect

A multi-center clinical study of granulocyte colony stimulating factor enhances survival in patients with liver failure and factors analysis that affect the therapeutic effect

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034366
Enrollment
Unknown
Registered
2020-07-03
Start date
2020-06-18
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

Liver Failure

Interventions

experimental group:G-CSF+Conventional treatments

Sponsors

The Fifth Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-65 years; (2) Signed informed consent; (3) The diagnosis of HBV-ACLF was made with reference to Acute-on-chronic liver failure: consensus recommendations of the Asian Pacific association for the study of the liver (APASL):an update and Update on Prevention, Diagnosis, and Treatment and of Chronic Hepatitis B:AASLD 2018 Hepatitis B Guidanceincluding a. basis of hepatitis B virus infection/hepatitis B/cirrhosis (positive the HBV surface antigen or serum HBVDNA for more than 6 months); b. Jaundice (serum bilirubin > 5mg/dL [>85umol/L]); c. coagulopathy (INR > 1.5 or prothrombin activity < 40%) without other causes; d. complicated within 4 weeks by ascites and/or encephalopathy; the severity of ACLF was assessed by the Model for End-Stage Liver Disease (MELD) (patients with MELD scores ranging 16-32 would be enrolled).

Exclusion criteria

Exclusion criteria: (1) Pregnant or lactating women; (2) Any detectable malignant tumor; (3) Bone marrow aplasia; (4) Concurrence of any other serious systemic diseases and psychiatric disorder (5) Recent or current participating in other clinical trial (6) Evidence of drug addiction during the last 1 year before enrollmen (7) Inability or unwillingness to sign the informed consent form or comply with the clinical trial requirements; (8) Any concurrent infection without effective anti-infection treatmen (10) Presentation of alcohol withdrawal symptom (11) Other virus co-infection; (12) Concurrence of cardiac,cerebral,or other system severe diseases.

Design outcomes

Primary

MeasureTime frame
Survival rates;

Secondary

MeasureTime frame
Incidence of adverse reactions;

Countries

China

Contacts

Public ContactJinhua Hu

The Fifth Medical Center of Chinese PLA General Hospital

13910020608@163.com+86 13910020608

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026