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Recruiting Observational

Reporting, Evaluating, Preventing and Treating the Cardiotoxicity Induced by Anticancer Drugs During a Specific Cardio-oncology Consult and Follow up in Routine Care

NCT03882580 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2019-03-01
Last updated
2026-09-11

Condition(s) studied

Cardiovascular ComplicationCardiovascular InsufficiencyCardiac ComplicationOncologic ComplicationsCardiac InsufficiencyMetabolic DisorderVascular DisorderCardiac Disorder

Investigational drug(s) / intervention(s)

Anti-Cancer Agents

Anti-Cancer Agents: Drugs and treatments used in cancer inducing cardiovascular and metabolic side effects

Study summary

Several Drugs used in routine care in oncology induce rare but often severe or fatal cardiovascular or metabolic side effects. This study will investigate, evaluate, report and treat the cardiovascular side effects of anticancer drugs, through a specific cardiovascular routine checkup and follow-up taking place in several Cardio-oncology programs throughout France. The different including centers will be: Assistance Publique - Hôpitaux de Paris (APHP.6: Pitié-Salpétrière, Saint Antoine and Tenon's hospitals, Paris, France).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Suffering a cancer * Evaluated within a cardio-oncology program Exclusion Criteria: * None

Primary outcome measure(s)

  • Number of patients having a benefit after this specific cardio-oncology check up and follow up — 5 years

Trial sites (3)

FacilityCityRegionStatus
AP-HP, Pitié-Salpêtrière Hospital, Department of Pharmacology, CIC-1421, Pharmacovigilance Unit, INSERM Paris France Recruiting
AP-HP, Saint-Antoine Hospital, Department of cardiology Paris France Recruiting
AP-HP, Tenon Hospital, Department of Cardiology Paris France Recruiting
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 NCT03882580 on ClinicalTrials.gov ↗ ← All trials in France