Atrial Fibrillation in Active Cancer Patients

NCT04696081 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2024-08-09

No results posted yet for this study

Summary

Atrial fibrillation is a common complication of both cancer and anticancer drugs but the consequences of such events remain poorly known and are not adressed in both phase III oncological trials and cardiological guidelines. The objective of this study is to create a prospective multicenter international registry of adult patients with an active cancer and experiencing atrial fibrillation to study major cardiovascular events occurrence during a 1 year follow-up.

Conditions

Interventions

OTHER

occurence of atrial fibrillation

all adult patients with an active cancer and experiencing atrial fibrillation will be consecutively include. Active cancers will be defined according Agnelli et al. (NEJM 2020; 382:1599-1607).

Sponsors & Collaborators

  • University Hospital, Marseille, France

    collaborator UNKNOWN
  • Hospices Civils de Lyon, France

    collaborator UNKNOWN
  • Centre Francois Baclesse, Caen, France

    collaborator UNKNOWN
  • University Hospital of Saint-Etienne, France

    collaborator UNKNOWN
  • Hôpital Lariboisière Fernand Widal, Paris, France

    collaborator UNKNOWN
  • Institut de Cancérologie de l'Ouest Nantes, France

    collaborator UNKNOWN
  • Fundacion Cardio Onco, Santiago, Chile

    collaborator UNKNOWN
  • Hunter New England Area Health Service, University of Newcastle, Australia

    collaborator UNKNOWN
  • University Hospital, Rouen

    collaborator OTHER
  • University Hospital, Caen

    lead OTHER

Principal Investigators

  • Joachim Alexandre, MD, PhD · Caen Normandy University Hospital, France

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2025-09-01
Completion
2026-01-01

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04696081 on ClinicalTrials.gov