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NCT07869329Not yet recruiting

Biomarker Testing to Predict Radiation-Related Heart Disease in Lung Cancer Patients

Predicting Radiation-induced Cardiac Disease With the Biomarker Serum Pro-N-Cadherin

Source: ClinicalTrials.gov · Last updated 9 Oct 2026

Brief summary (registry, in English)

The study will measure serum Pro-N-Cadherin and NT-proBNP (pro B-type natriuretic peptide) levels in adults with non-small cell lung cancer receiving hypofractionated radiation therapy and evaluate whether these biomarkers correlate with radiation dose to the heart, cardiac dysfunction, and adverse cardiac events. Participants will undergo blood collection and echocardiography over a two-year follow-up period.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
6 Oct 2026
Start date
Nov 2026
Primary completion date
Nov 2030
Lead sponsor
Duke University
Diseases
Lung cancer
NCT number
NCT07869329

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From Nov 2026 to the primary completion date, Nov 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Planning to receive concurrent or sequential chemotherapy or immunotherapy
  • Prior radiation therapy to the chest that included more than a minimal dose to the heart (\> 1 Gy mean dose).

Who the study is looking for

  • ≥ 18 years of age
  • Histologic documentation or clinical suspicion of non-small cell lung cancer based on pathology or imaging.
  • Location of disease must be either a central right-sided tumor (defined as tumors with a planning target volume within 2 cm of the primary airways) arising below the level of the heart or any left-sided tumor arising below the level of the heart.
  • Planned to receive hypofractionated radiation therapy (4-18 Gy fractions to a total dose of 45-70 Gy)
  • Planning the target volume that is at or below the most superior aspect of the heart.
  • Willing and able to provide written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Duke University Medical Center
Coordinator of this site? Confirm its status
DurhamUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.