Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
Healthy Volunteers
NCT06628102

Improving Detection of Early Lung Cancer in a Diverse Population (IDEAL) Study

Led by British Columbia Cancer Agency · Updated on 2024-10-04

3600

Participants Needed

1

Research Sites

282 weeks

Total Duration

On this page

Sponsors

B

British Columbia Cancer Agency

Lead Sponsor

L

Laval University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this trial is to (a) identify people at high risk of lung cancer who would benefit from LDCT screening but are currently ineligible based on current lung cancer screening criteria (b) provide the framework to manage patients with Incidental Pulmonary Nodules (IPNs) with appropriate follow-up based on accurate interpretation of the Chest CT scan that is already available and (c) develop a simple, point-of-care, minimally invasive test, focusing on the breath and circulating blood proteins, to detect lung cancer, and develop a method to differentiate between cancerous and non-cancerous nodules using a single. Participants will be asked to answer a questionnaire regarding their age, race/ethnicity, smoking history, and residential history if they have ever been told they have chronic obstructive pulmonary disease (COPD), high blood pressure, education level, medications and height and weight. Participants will then be asked to give a breath sample via the breath collection device. All this information will be collected before the breath collection. After that, participants will give 1-2 tablespoons of blood. CT scans with IPN(s) will be reviewed and run through a computer detection software to identify nodules, followed up as per current clinical guidelines.

CONDITIONS

Official Title

Improving Detection of Early Lung Cancer in a Diverse Population (IDEAL) Study

Who Can Participate

Age: 50Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 50 to 80 years
  • Able to provide consent
  • Chest CT scan shows nodule 6mm or larger
  • No other cancers except lung cancer for group 1
  • Must abstain from smoking tobacco for 24 hours before breath test
Not Eligible

You will not qualify if you...

  • Too sick to provide a breath sample
  • Smoked tobacco in the last 24 hours
  • Pregnant
  • Diagnosed with a respiratory infection in the last 3 months
  • Unwilling to consent to the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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+1

Trial Site Locations

Total: 1 location

1

BC Cancer Research, part of the Provincial Health Authority

Vancouver, British Columbia, Canada, V6K 2N2

Actively Recruiting

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Research Team

R

Renelle L Myers, MD

CONTACT

C

Crista L Bartolomeu, 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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