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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06233708
Other study ID # 2023-0713
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2008
Est. completion date May 31, 2022

Study information

Verified date January 2024
Source Asan Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 2092
Est. completion date May 31, 2022
Est. primary completion date May 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Non-Selective Beta-Adrenoreceptor Agonists for Systemic Use
Non-selective blocker including Propranolol, Carvedilol PO was prescribed

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Asan Medical Center Korea Health Industry Development Institute

Outcome

Type Measure Description Time frame Safety issue
Primary Kaplan-Meier survival analysis of HCC recurrence at 5-year follow-up HCC 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. Baseline and 5-year follow-up
Primary Multivariate Cox regression analysis of HCC recurrence at 5-year follow-up Multivariate Cox regression analysis was performed to identify the risk factors for HCC recurrence. Baseline and 5-year follow-up
Secondary Kaplan-Meier survival analysis of overall survival at 5-year follow-up Overall survival was collected and compared using Kaplan-Meier survival analysis. Baseline and 5-year follow-up
Secondary Multivariate Cox regression analysis of overall survival at 5-year follow-up Multivariate Cox regression analysis was performed to identify the risk factors for overall mortality. Baseline and 5-year follow-up
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