Clinical Trials in Australia / NCT04962711
Recruiting Not applicable

Risk-guided Disease Management Plan to Prevent Heart Failure in Patients Treated With Previous Chemotherapy (REDEEM)

NCT04962711 · tracked via the Priya Life Science Australia tracker
Phase
Not applicable
Started
2023-03-30
Last updated
2025-05-31

Condition(s) studied

Heart Failure

Investigational drug(s) / intervention(s)

Heart Failure intervention (Cardio-Oncology Disease Management Plan (CO-DMP)Usual care

Heart Failure intervention (Cardio-Oncology Disease Management Plan (CO-DMP): A clinical review to ensure optimal risk factor control and cardioprotection along with exercise intervention.

Usual care: provided by participants' usual healthcare professional(s)

Study summary

This is a prospective study in which a process of identifying and reducing heart failure (HF) risk will be applied to cancer survivors \>55 years old with chemotherapy \>5 years ago.

The overall goal of this study to identify the feasibility and value of risk-guided cardiac rehabilitation (exercise, risk factor modification, and behavioural support) as a component of survivorship care.

Eligibility

Sex
ALL
Min age
40 Years
Max age
85 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. History of cancer \> 10 years ago 2. Have received potentially toxic chemotherapy Anthracycline (any dose) Trastuzumab (Herceptin) in breast-cancer with the HER2 mutation OR Tyrosine kinase inhibitors (e.g. sunitinib) OR Left chest radiotherapy Exclusion Criteria: 1. Ejection fraction at baseline echo \<50% 2. Valvular stenosis or regurgitation of \>moderate severity 3. History of previous heart failure (baseline New York Heart Association (NYHA) classification \>2) 4. Systolic BP \<110 mmHg 5. Pulse \<60/minute if not on beta blocker 6. Inability to acquire interpretable images (identified from baseline echo) 7. Contraindications to beta blockers or angiotensin-converting enzyme inhibitors 8. 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 9. Already taking both angiotensin converting enzyme inhibitors/angiotensin receptor blockers and beta blockers, or intolerance (or allergy) to both. 10. Unable to provide written informed consent to participate in this study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Baker Heart and Diabetes Institute Melbourne Victoria Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04962711 on ClinicalTrials.gov ↗ ← All trials in Australia