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A prospective randomized study on the efficacy of two nucleoside (acid) analogue against hepatitis B recurrence after liver transplantation

A prospective randomized study on the efficacy of two nucleoside (acid) analogue against hepatitis B recurrence after liver transplantation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-PRC-10001092
Enrollment
Unknown
Registered
2010-06-02
Start date
2010-06-01
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

Hepatitis B recurrence after liver transplantation

Interventions

1:NA plus NA

Sponsors

First Central Hospital, Tianjin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (Long-term survival group): Hepatitis B related end-stage liver disease patients undergoing liver transplantation; Have been receiving HBIG combined nucleoside (acid) analogue treatment to prevent hepatitis B recurrence; Survival time > 3 years after liver transplantation; No recurrence of hepatitis B; Aged 18 to 65 years old; Able and willing to provide signed informed consent. (Early postoperative group): Hepatitis B related end-stage liver disease patients undergoing liver transplantation; Able and willing to provide signed informed consent; Survival time > 6 months after liver transplantation.

Exclusion criteria

Exclusion criteria: (Long-term survival group): Withdrew from the study by himself/herself; Stop HBIG and (or) nucleotides (acid) analogues to prevent recurrence of hepatitis B virus by himself/herself; Exogenous hepatitis B virus infection after liver transplantation. (Early postoperative group): Hepatitis B antigen of the donor is positive; Withdrew from the study by himself/herself; Stop HBIG and (or) nucleotides (acid) analogues to prevent recurrence of hepatitis B virus by himself/herself; Exogenous hepatitis B virus infection after liver transplantation

Design outcomes

Primary

MeasureTime frame
HBV-DNA, HBs-Ag, HBS-Ab, HBeAg, HBeAb, HBcAb, ALT, AST, TB, GGT, ALP, liver bioposy;

Countries

China

Contacts

Public ContactLiying Sun
sunxlx@yahoo.com.cn+86 13502038977

Outcome results

None listed

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