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Risk-guided Disease managEment Plan to prevEnt CAD in Patients Treated With Previous Cancer (REDEEM-CAD)

B

Baker Heart and Diabetes Institute

Status

Enrolling

Conditions

Coronary Artery Disease

Treatments

Diagnostic Test: Coronary CT

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

REDEEM-CAD is a prospective multi-centre study of CAD risk evaluation and management in cancer survivors 40-70 years with chemotherapy or radiotherapy >5 years ago.

Full description

REDEEM-CAD is a prospective multi-centre study in which a process of evaluating the risk of coronary artery disease is studied in cancer survivors 40-70 years with chemotherapy or radiotherapy >5 years ago. The efficacy of this CAD risk evaluation will be compared with the broad community in two existing studies - CAUGHT-CAD and EDCAD. This unique Screening/Management Plan (SMP) has 2 components; 1) A novel clinical and imaging-based screening algorithm to select those most likely to develop coronary artery disease, 2) A clinical review to ensure optimal risk factor control and cardio protection.

Follow-up of treated patients will continue for an average of 36 months, with clinic reviews at 12, 24 and 36 months. The results will define the prevalence of subclinical coronary artery disease, and the feasibility and the efficacy of the SMP.

Enrollment

748 estimated patients

Sex

All

Ages

40 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

A history of cancer >5 y ago associated with potential cardiotoxicity from chemotherapy and/or radiotherapy (chiefly survivors of breast cancer, Hodgkin's lymphoma and prostate cancer).

Exclusion criteria

  • Unable to provide written informed consent to participate in this study
  • Known coronary artery disease at recruitment
  • History of previous coronary artery disease
  • Inability to acquire interpretable CT images
  • Contraindications/Intolerance to or already taking statin therapy
  • Oncologic (or other) life expectancy <12 months or any other medical condition (including pregnancy) that results in the belief (deemed by the Chief Investigators) that it is not appropriate for the patient to participate in this trial

Trial design

748 participants in 2 patient groups

Survivor Screening/Management Plan
Description:
In cancer survivors; 1. A novel clinical and CT imaging-based screening algorithm to select those most likely to develop coronary artery disease, 2. A clinical review to ensure optimal risk factor control and cardiac protection.
Treatment:
Diagnostic Test: Coronary CT
Non-cancer Screening/Management Plan
Description:
In matched non-cancer patients (from EDCAD trial); 1. A novel clinical and CT imaging-based screening algorithm to select those most likely to develop coronary artery disease, 2. A clinical review to ensure optimal risk factor control and cardiac protection.
Treatment:
Diagnostic Test: Coronary CT

Trial contacts and locations

2

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Central trial contact

Lisa Riddell; Tom Marwick, MBBS,PhD,MPH

Data sourced from clinicaltrials.gov

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