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

NCT06628102 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3600

Last updated 2024-10-04

No results posted yet for this study

Summary

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

Interventions

DIAGNOSTIC_TEST

Chest CT Scan

Chest CT Scan

Sponsors & Collaborators

  • Laval University

    collaborator OTHER
  • Lunenfeld Tanenbaum Research Institute

    collaborator OTHER
  • Canadian Cancer Society (CCS)

    collaborator OTHER
  • University Health Network, Toronto

    collaborator OTHER
  • British Columbia Cancer Agency

    lead OTHER

Principal Investigators

  • Renelle L Myers, MD · VCH, UBC

  • Rayjean Hung, PhD · Sinai Health

Study Design

Allocation
NA
Purpose
SCREENING
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-08-04
Primary Completion
2028-12-31
Completion
2028-12-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06628102 on ClinicalTrials.gov