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Association Between Pre-op Non-Selective Beta-Blockers and Hepatocellular Carcinoma Recurrence Post-Liver Transplant

A

Asan Medical Center

Status

Completed

Conditions

Hepatocellular Carcinoma Recurrent
Hepatocellular Carcinoma

Treatments

Drug: Non-Selective Beta-Adrenoreceptor Agonists for Systemic Use

Study type

Observational

Funder types

Other

Identifiers

NCT06233708
2023-0713

Details and patient eligibility

About

The goal of this observational study is to investigate the effect of non-selective beta-blocker (NSBB) on the recurrence of hepatocellular carcinoma (HCC) following liver transplantation in patients who underwent liver transplantation (LT) for treating hepatocellular carcinoma.

The main question[s] it aims to answer are:

  • Is the usage of non-selective beta-blocker associated with decreased recurrence of hepatocellular carcinoma following liver transplantation?
  • Is the usage of non-selective beta-blocker associated with all-cause mortality following liver transplantation?

Researchers will compare the NSBB group, including patients who received non-selective beta-blocker therapy for at least 30 consecutive days within 3 months prior to liver transplantation more than 30 days prior, with the control group to to see if non-selective beta-blocker treatment is associated with decreased recurrence of hepatocellular carcinoma following liver transplantation.

Enrollment

2,092 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients
  • Underwent liver transplantation for treating hepatocellular carcinoma
  • Between Jan. 2008 - May. 2022

Exclusion criteria

  • Pediatric patients (Age under 18 years)
  • Re-transplantation
  • Multi-organ transplantation

Trial design

2,092 participants in 2 patient groups

NSBB group
Description:
The NSBB group was defined as those who received NSBBs for at least 30 consecutive days within the 3 months prior to LT.
Treatment:
Drug: Non-Selective Beta-Adrenoreceptor Agonists for Systemic Use
Control group
Description:
Those who did not meet the above criteria were classified as the control group.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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