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Signature Development and Validation Protocol for an Epigenetic Assay in Diagnosing Lung Cancer

Signature Development and Validation Protocol for an Epigenetic Assay in Diagnosing Lung Cancer

Recruiting
18 years and older
All
Phase N/A

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Overview

The purpose of this research study is to test a new process for diagnosing lung cancer by examining changes to your DNA that can be detected from a blood test. The information we learn by doing this study could potentially help people in the future.

Participants in this study will have blood samples collected, have their medical records reviewed by study personnel and fill out questionnaires at different time points during the study. Blood sample collection will occur during normal routine clinic visits. Participation in this study will last approximately 5 years.

Description

This clinical testing research study outlines the validation process for an epigenetic assay targeting host peripheral blood cell and the associated host DNA methylation signatures designed to diagnose lung cancer. The overall protocol process will involve three distinct stages representing three patient cohorts with up to 250 subjects per cohort across 5 populations of patients. Cohort one will act as signature development phase; cohort two will act as signature finalization phase; and cohort three will act as a validation cohort phase. Each cohort will include the following patient populations with up to 50 patients per population:

  1. Lung cancer; No chemotherapy. Surgical resection or stereotactic body radiation therapy (SBRT) only
  2. Lung cancer; With chemotherapy. All stages including remission
  3. At risk group (Lung cancer screening population)
  4. Control group with mixed comorbid disease EXCLUDING tobacco use of greater than 10 pack years (PY) or chronic obstructive pulmonary disease (COPD)
  5. Healthy controls with no comorbid disease

Eligibility

Inclusion Criteria:

  • 18 years old or older
  • Patient at University of Maryland Baltimore Washington Medical Center
  • Willing and able to consent to study procedures listed in the protocol
  • Ability to speak and understand English

Exclusion Criteria:

  • Younger than 18 years old
  • Patient not cared for at University of Maryland Baltimore Washington Medical Center
  • Unable to consent to study procedures listed in the protocol
  • Unable to speak or understand English

Study details
    Lung Cancer
    Lung Cancer Screening
    Healthy Volunteers (HV)
    Unhealthy Volunteers

NCT07008664

University of Maryland, Baltimore

17 June 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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