Statins and ACE Inhibitors for Heart Protection in Cancer Patients

Pharmacologic Therapies to Mitigate Radiation- Associated Heart Disease

Recruiting Phase 2 Interventional Study
Chest Wall Tumor Breast Cancer Lung Cancer Esophageal Cancer Mediastinal Cancers Spine Metastases Spinal Tumor Thoracic Cancer Thoracic Neoplasms
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Supportive Care
Participants needed
60 (estimated)
Sponsor
UNC Lineberger Comprehensive Cancer Center · Other
Who this trial is looking for

This trial is looking for adult patients receiving radiation therapy for certain chest tumors. Participants will take either a statin or an ACE inhibitor to see if it helps protect their heart from damage caused by radiation.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am at least 18 years old
  • I can give written consent to participate
  • I agree to provide blood samples
  • I am willing to follow study procedures

You may not be able to join if

  • I am pregnant or breastfeeding
  • I already take a statin or ACE inhibitor
  • I have low blood pressure

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial
Radiation therapy is an essential treatment for tumors in the chest area, including breast, lung, esophageal, mediastinal cancers, and spine metastases. Although technical advances have reduced treatment-related illness and death, radiation exposure to the heart can still cause substantial rates of radiation-induced heart disease (RIHD) among survivors. For example, about 21% of non-small cell lu…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Written informed consent obtained to participate in the study and HIPAA * authorization for release of personal health information. * Subjects is willing and able to comply with study procedures based on the * judgement of the investigator. * Consent for serial blood draws and…
Contacts

Claire Kowalczyk

984-974-0000

claire_kowalczyk@med.unc.edu

CONTACT