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NCT05227261Completed

Early Detection of Five Common Cancers Using the ctDNA Analysing Test

Assessment of a Novel Blood Test in Early Detection of the Five Common Cancers Based on the Investigation of the Circulating Tumour DNA

Source: ClinicalTrials.gov · Last updated 18 Feb 2025

Brief summary (registry, in English)

This is a multi-centre, prospective cohort study, aiming to evaluate a blood test in early detection of the four common cancers, based on the investigation of the circulating tumour DNA (ctDNA). Primary objective: To evaluate the performance characteristics of the blood ctDNA test in early detecting cancers. Secondary objectives: * To evaluate the performance characteristics of the test in determining the origin of tumour, as compared to the findings of the imaging diagnostic tests. * To determine the risk of cancers development in the high-risk population, as compared to that in the moderate-risk group.

Status (registry)
Completed
Study type
Observational
Enrollment
9057 (actual)
First submitted
26 Jan 2022
Start date
Apr 2022
Primary completion date
Apr 2023
Lead sponsor
Gene Solutions
NCT number
NCT05227261

What you commit to

  • Study type: Observational
  • Participants enrolled: 9057
  • From Apr 2022 to the primary completion date, Apr 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of cancer (cancer has either been confirmed or been treated within the past 3 years)
  • History of blood transfusion or bone marrow transplantation within the past 3 years

Other

  • Does not agree to participate in study
  • The subject has clinical manifestations of pregnant.

Who the study is looking for

  • Aged 40 or above at enrolment
  • Neither clinical suspicion of cancer nor history of confirmed cancer has been reported
  • Agree to be contacted at 6 months and 12 months following enrolment to collect information about general health status and progress of cancer (if possible)
  • Provide written informed consent

Age in the registry: 40 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hanoi Medical University
Coordinator of this site? Confirm its status
HanoiVietnamUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.