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NCT07358715Recruiting

Liquid Biopsy-Based Pre-Screening to Streamline LDCT Lung Cancer Screening in High-Risk Individuals

A Multimodal Liquid Biopsy-Based Assay as a Pre-Screening Test Before Low Dose CT Thorax (LDCT) to Streamline Lung Cancer Screening in High-Risk Individuals

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

This study evaluates the feasibility and cost-effectiveness of using a blood-based liquid biopsy assay as a pre-screening tool before low-dose CT (LDCT) for lung cancer screening. By identifying individuals unlikely to have lung cancer, this approach aims to reduce unnecessary LDCT scans, radiation exposure, and healthcare costs, while improving early detection, particularly among high-risk individuals including never-smokers with a family history of lung cancer.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
140 (estimated)
First submitted
6 Jan 2026
Start date
1 Nov 2024
Primary completion date
31 Dec 2027
Lead sponsor
National University Hospital, Singapore
Diseases
Lung cancer
NCT number
NCT07358715

What you commit to

  • Study type: Interventional
  • Planned participants: 140
  • From 1 Nov 2024 to the primary completion date, 31 Dec 2027
  • 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.

Prior treatment

  • Prior low-dose CT (LDCT), CT thorax, or PET-CT performed within 12 months prior to enrollment
    • Lung Cancer Cohorts Only

Other illness

  • Known allergy or contraindication to CT contrast agents
  • Receipt of any prior cancer-directed treatment for lung cancer

Other

  • Applicable to All Participants
  • Pregnant or breastfeeding women
  • Inability or unwillingness to comply with study procedures
    • High-Risk Individuals Only

Who the study is looking for

  • High-Risk Individuals (n = 100)
  • No prior history of lung cancer
  • Meets one of the following high-risk definitions:
    • Current or former smoker (quit within the past 15 years), aged 55-74 years, with a smoking history of ≥30 pack-years; OR
    • Never-smoker aged 55-75 years with a first-degree family history of lung cancer
  • Able and willing to provide written informed consent
    • Early-Stage Lung Cancer Patients (n = 20)
  • Aged ≥21 years
  • Histologically or clinically confirmed stage I-II lung cancer
  • Treatment-naïve (no prior surgery, chemotherapy, radiotherapy, or immunotherapy for lung cancer)
  • Able and willing to provide written informed consent
    • Advanced-Stage Lung Cancer Patients (n = 20)
  • Aged ≥21 years
  • Histologically or clinically confirmed stage III-IV lung cancer
  • Treatment-naïve (no prior systemic or local therapy for lung cancer)
  • Able and willing to provide written informed consent

Age in the registry: 21 years to 75 years · 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
National University Hospital Singapore
Coordinator of this site? Confirm its status
SingaporeSingaporeRecruiting

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