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NCT06304857

CardioPROTECTion with Dapagliflozin in Breast Cancer Patients Treated with AnthrAcycline - PROTECTAA TRIAL

Recruiting · Phase 3 · 4th Military Clinical Hospital with Polyclinic, Poland · registry updated 2024-12-04

Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.

The purpose of this study is to evaluate the effect of dapagliflozin on the incidence of cancer therapeutics-related cardiac dysfunction in patients with breast cancer receiving anthracycline treatment.

Inclusion

  • Age \> 18 years and \< 80 years.
  • Diagnosis of invasive breast cancer \[stage I-III\] and planned anthracycline treatment within 60 days.
  • Signed Informed Consent to participate in the study.

Exclusion

  • Urinary tract infection with the need for treatment with an antibiotic 48 hours before the scheduled start of anthracycline treatment.
  • Recognised heart failure or symptoms which, in the opinion of the investigator may be a symptom of undiagnosed heart failure.
  • Left ventricular ejection fraction \< 50% at the time of the screening.
  • Severe valvular heart disease.
  • A history of clinically significant arrhythmia, including atrial fibrillation regardless of type (at discretion of the investigator).
  • A history of stroke.

Open NCT06304857 on ClinicalTrials.govAll conditions

CardioPROTECTion with Dapagliflozin in Breast Cancer Patients Treated with AnthrAcycline - PROTECTAA TRIAL | Clinical Trial Matcher