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

Association Between Pre-operative Use of Non-selective Beta-blockers With the Risk of Hepatocellular Carcinoma Recurrence Following Liver Transplantation : a Retrospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06233708
Enrollment
2092
Registered
2024-01-31
Start date
2008-01-01
Completion date
2022-05-31
Last updated
2024-01-31

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

Conditions

Hepatocellular Carcinoma, Hepatocellular Carcinoma Recurrent

Brief summary

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.

Interventions

DRUGNon-Selective Beta-Adrenoreceptor Agonists for Systemic Use

Non-selective blocker including Propranolol, Carvedilol PO was prescribed

Sponsors

Korea Health Industry Development Institute
CollaboratorOTHER_GOV
Asan Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Kaplan-Meier survival analysis of HCC recurrence at 5-year follow-upBaseline and 5-year follow-upHCC recurrence, which was diagnosed based on pathological or radiographic evidence of new lesions consistent with HCC, and recurrence-free survival was collected and compared using Kaplan-Meier survival analysis.
Multivariate Cox regression analysis of HCC recurrence at 5-year follow-upBaseline and 5-year follow-upMultivariate Cox regression analysis was performed to identify the risk factors for HCC recurrence.

Secondary

MeasureTime frameDescription
Kaplan-Meier survival analysis of overall survival at 5-year follow-upBaseline and 5-year follow-upOverall survival was collected and compared using Kaplan-Meier survival analysis.
Multivariate Cox regression analysis of overall survival at 5-year follow-upBaseline and 5-year follow-upMultivariate Cox regression analysis was performed to identify the risk factors for overall mortality.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026