Actively Recruiting

Phase Not Applicable
Age: 55Years - 74Years
All Genders
Healthy Volunteers
NCT06016569

Study of Early Cancer Biomarkers in Breath Condensate in Population of Individuals With High-Risk of Lung Cancer Undergoing LDCT Screening.

Led by The Institute of Molecular and Translational Medicine, Czech Republic · Updated on 2026-02-12

3200

Participants Needed

3

Research Sites

391 weeks

Total Duration

On this page

Sponsors

T

The Institute of Molecular and Translational Medicine, Czech Republic

Lead Sponsor

C

Cancer Research Foundation CR

Collaborating Sponsor

AI-Summary

What this Trial Is About

The trial will evaluate if the newly identified biomarkers of lung cancer in exhaled breath condensate are as a diagnostic tool comparable to the low-dose computer tomography (LDCT) implemented in lung cancer screening recently. Due to the possibility to collect breath condensate at any medical workplace and due to the relatively low financial cost of examination of the collected breath condensate could improve early diagnosis of lung cancer, differential diagnostics of lung nodules and thereby reduce both the unnecessary interventions and deaths from this type of cancer.

CONDITIONS

Official Title

Study of Early Cancer Biomarkers in Breath Condensate in Population of Individuals With High-Risk of Lung Cancer Undergoing LDCT Screening.

Who Can Participate

Age: 55Years - 74Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Consent to participate in the clinical trial
  • Age between 55 and 74 years
  • Current smoker or ex-smoker with at least 20 pack-years of smoking history
  • Priority given to those with at least 30 pack-years of smoking
  • Preference for former smokers who quit less than 15 years ago
Not Eligible

You will not qualify if you...

  • Previous diagnosis of lung cancer
  • Ongoing symptomatic treatment for active malignant tumor
  • Advanced dementia
  • Chronic obstructive pulmonary disease or other inflammatory lung disease in acute exacerbation

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Masaryk Memorial Cancer Institute

Brno, Czechia, 65653

Actively Recruiting

2

University Hospital

Olomouc, Czechia, 77900

Not Yet Recruiting

3

General University Hospital in Prague

Prague, Czechia, 12808

Not Yet Recruiting

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Research Team

M

Marian Hajduch, MD, PhD.

CONTACT

M

Michaela Bendova, MSc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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