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Multiple-center clinical study of Antiviral Treatment with Nucleoside Analogues on Patients with HBV Associated Acute on Chronic Liver Failure among Multiple Center

Multiple-center, randomized, open and parallel controlled clinical trail of Nucleoside Analogues: effect and safty on patients with HBV Associated Acute on Chronic Liver Failure

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12001980
Enrollment
Unknown
Registered
2012-02-16
Start date
2008-11-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

HBV associated acute on chronic liver failure

Interventions

B:lamivudine

Sponsors

Liver Failure Treatment and Research Center, 302 Military Hospital ,Beijing, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) age 16-65, male or female; (2) HBVDNA positive; (3) No antiviral therapy with nucleoside analogues within six months; (4) HBV associated ACLF was diagnosed according to the national clinical guidelines on liver failure (issued in 2006)12, including TBil>170umol/L or daily increase >=17umol/L, and PA from 20% to 40%, with or without hepatic encephalopathy below IIo and ascites.

Exclusion criteria

Exclusion criteria: (1) terminal-stage patients with PA<20%, or with severe complications should be excluded, such as hepatic-renal syndrome, severe infection, massive hemorrhage of the digestive tract, and refractory electrolyte disturbances; (2) Concurrent viral infection should be excluded, including HAV, HCV, HDV, HEV, HIV, CMV, EBV etc.; (3) Liver failure caused by other reasons should be excluded (including autoimmune diseases, alcoholic or drug-related); (4) unsuited community women in pregnancy and lactation; (5) malignant tumors were excluded; (6) patients with other severe systematic diseases and mental diseases were excluded.

Design outcomes

Primary

MeasureTime frame
survival rate;

Secondary

MeasureTime frame
liver function;HBVDNA;

Countries

China

Contacts

Public ContactWang Huifen
wanghuifen@mednail.com.cn+86 10 66933012

Outcome results

None listed

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