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NCT Number: NCT05366153

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

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.

Recruiting

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Key information

Age range

40 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Tom Marwick, Hobart, Tasmania, Australia

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Coronary CT

Diagnostic Test

Screening/Management Plan

Primary outcomes

  1. Proportion of evaluated patients who should undergo CAD prevention

    Time frame: 3 years

    High clinical risk, or intermediate risk with CAC score >0

Secondary outcomes

  1. Proportion with critical CAD

    Time frame: 3 years

    Coronary stenosis >70% by CT coronary angiogram

  2. Proportion at intermediate clinical risk

    Time frame: 3 years

    Intermediate clinical risk (0.8-2.0% annualized risk by Pooled Cohort Equation)

  3. Statin responsiveness

    Time frame: 3 year follow-up

    Change in plaque volume

Study contacts

Contact information is provided by the study sponsor or research team.

Lisa Riddell

CONTACT

[email protected]

+61 3 8532 1550

Tom Marwick, MBBS,PhD,MPH

CONTACT

[email protected]

+61 3 8532 1550

Sponsors and collaborators

Lead sponsor

Baker Heart and Diabetes Institute

Other

Collaborators

  • Menzies Institute for Medical Research
  • Northern Hospital, Australia
  • Peter MacCallum Cancer Centre, Australia
  • The Alfred
  • Western Health, Australia

Registry information

Official study title

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

Acronym: REDEEM-CAD

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
May 9, 2022
Registry last updated
Dec 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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