RecruitingNot ApplicableNCT04782557

EUS Guided HVA and PVA for Circulating Tumor DNA in Patients

Endoscopic Ultrasound Guided Hepatic and Portal Vein Aspiration for Circulating Tumor DNA in Patients Suffering From GI Cancers


Sponsor

Chinese University of Hong Kong

Enrollment

60 participants

Start Date

Jan 1, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

The discovery of cell-free circulating tumor DNA (crDNA) in blood and the maturation of technologies for ctDNA analysis have presented an attractive opportunity for minimally invasive "liquid biopsy" genomic diagnostics. The investigators plan to perform EUS-guided portal vein and hepatic vein aspiration in GI cancers patients. The aim of the current study is thus to examine the concentration of ctDNA in portal vein (EUS-guided PVA), hepatic vein (EUS-guided HVA) and peripheral blood to understand the first pass effect of the liver with gastrointestinal (GI) cancers, and the possibility of using ctDNA as a marker for preoperative staging, restaging after neoadjuvant chemotherapy, and monitoring for recurrence.


Eligibility

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying EUS-guided portal vein and hepatic vein aspiration for people with circulating tumor cell and gastrointestinal cancer. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTEUS-guided portal vein and hepatic vein aspiration

EUS-guided portal vein and hepatic vein aspiration


Locations(1)

The Chinese University of Hong Kong

Hong Kong, Hong Kong

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NCT04782557


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