Actively Recruiting
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
Eligibility Criteria
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
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
Trial Site Locations
Total: 1 location
1
BC Cancer Research, part of the Provincial Health Authority
Vancouver, British Columbia, Canada, V6K 2N2
Actively Recruiting
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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