CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 403 enrolled
Drug / intervention
ctDNA methylation in and it's Correlation wth Development and prediction of HCCother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03483922
NCT03483922N/ACompleted

Clinical Trials on Detection of Hepatocellular Carcinoma With Non-invasive Method Based on DNA Methylation of Circulated Tumor DNA, PBMC and T Cells

HKGepitherapeutics·observational·Posted Mar 30, 2018·Updated Jul 5, 2024

In Brief

An observational study evaluating ctDNA methylation in and it's Correlation wth Development and prediction of HCC for Hepatocellular Carcinoma. Completed, enrolled 403 participants across 1 site.

Detailed Summary

Hepatocellular Carcinoma (HCC) is the fifth most common cancer world-wide. It is particularly prevalent in Asia, and its occurrence is highest in areas where hepatitis B is prevalent, indicating a possible causal relationship. Follow up of high-risk populations such as chronic hepatitis patients and early diagnosis of transitions from chronic hepatitis to HCC would improve cure rates. In most cases HCC is detected late resulting in increased mortality and morbidity. The purpose of this study is to develop and test non-invasive biomarkers based on methylation changes in PBMC and circulated tumor DNA in hepatocellular carcinomas patients.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesBangladesh

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedMar 30, 2018
Enrollment StartAug 20, 2018
Primary CompletionJun 1, 2020
Study CompletionNov 1, 2020
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 8.3 years ago

Interventions

ctDNA methylation in and it's Correlation wth Development and prediction of HCCother

Blood sample from patients with HCC, healthy individuals and individuals with hepatitis B will be collected, and DNA will extracted from PBMC and circulated tumor DNA will be subjected to bisulfite conversion. DNA from PBMC DNA will be analyzed with primers developed for the AHNAK-STAP1 genes. Plasma samples will be subjected to EZ direct DNA extraction and bisulfite conversion kit and will be amplified with primers developed to amplify the target regions. DNA will be used for the subsequent PCR amplification with specific primer to generate PCR amplicon for sequencing using a double PCR procedure. The product of PCR reaction will be subjected to indexed MiSeq Next-Generation sequencing that will allow us quantify DNA methylation level.