ClinicalTrials.Veeva

Menu

Cardiovascular Outcome of Cancer Patients: The "GMEDICO Cohort"

P

Public Assistance-Hospitals of Marseille (AP-HM)

Status

Enrolling

Conditions

Cardiovascular Prognosis

Treatments

Biological: blood samples

Study type

Interventional

Funder types

Other

Identifiers

NCT03492528
2017-A03362-51 (Other Identifier)
2017-50

Details and patient eligibility

About

The Mediterranean Group of Cardio-Oncology (GMEDICO) brings together French cardiologists and oncologists who have developed a protocol for the monitoring and cardio-oncological management of patients treated for cancer.

This unique organization makes it possible to envisage the creation of a large cohort from which the incidence and predictive factors of cardiovascular toxicity can be determined.

Primary objective: to determine the cardiovascular prognosis of patients treated for cancer and followed up in cardio-oncology.

Secondary objectives

  • To determine the clinical, biological and imaging factors associated with cardiovascular events under cancer treatment, in order to define a risk score including clinical, biological (biomarker) and imaging data.
  • To create a biological source for testing other biomarkers and conducting genome-wide association studies and genetic factors associated with cardiovascular events under cancer treatment.

Full description

Each patient will be monitored for 5 years. Cardio-oncological follow-up and management within these centers will follow a common protocol established and validated in March 2016 on the basis of international recommendations and summaries of the characteristics produced for each drug. Additional blood samples will be taken for the biobanking. Depending on the case, a small skin biopsy will be carried out to analyze the cardiovascular response of in vitro immunotherapy using a reprogramming model of fibroblasts in hiPSC hiPSC (human induced Pluripotent Stem cells)-cardiomyocytes.

Enrollment

530 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All adults referred for specialist cardio-oncology consultations before the initiation of a cancer treatment according to pre-established indications will be eligible.

Exclusion criteria

  • Failure to provide information that makes it impossible to complete a consultation form or refuse to sign the consent.
  • Minor or major patient under guardianship
  • Pregnant or breastfeeding woman

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

530 participants in 1 patient group

Cardiovascular patients treated for a cancer
Experimental group
Treatment:
Biological: blood samples

Trial contacts and locations

1

Loading...

Central trial contact

franck thuny

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems