Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03678337
Other study ID # 2018-A00429-46
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 26, 2019
Est. completion date January 2021

Study information

Verified date August 2018
Source University Hospital, Caen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Recently, the medical management of cancer patients has considerably improved the prognosis of these patients and today some cancers are becoming "chronic diseases". As a result, new adverse effects (AEs) are observed, particularly cardiac.

These "new" cardiac AEs are the consequence of a significant increase in patients life expectancy (delayed AEs not previously seen) but also the use of new pharmacological classes of anticancer drugs such as kinase inhibitors. The incidence of these cardiac AEs varies according to the patient profile and the anticancer molecules used, but their impact on the morbidity and mortality of the patients is significant.

In this context, we started at the University Hospital of Caen Normandy in September 2017 a cardio-oncology program entitled "prevention and pharmacological management of cardiac adverse effects induced by drugs used in Oncology" (PICARO program). This program involves the pharmacology department (opening of a dedicated consultation), the cardiology department (opening of a dedicated ultrasound consultation), vascular medicine departement (opening of a dedicated consultation) and the oncology federation. This program aims to be regional in the future. We therefore propose to build a cohort backed up to the PICARO program to assess the regional impact of cardiac AEs of anticancer drugs and thus to be better able to specify the number of AEs, the incidence and regional prevalence of these drugs. .

The constitution of this cohort is only the first step towards the constitution in the near future (2 years) of an observatory and then a regional registry of cardiac AEs induced by anticancer drugs. The objectives associated with the establishment of such a registry would be to reduce the number of cardiac AEs, the hospitalizations caused by these AEs, a better information of health professionals and patients, an improvement in the screening of patients at risk, all coming back in the context of health, clinical, epidemiological and pharmacological surveillance.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date January 2021
Est. primary completion date September 10, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient = 18 years,

- Attents of cancer,

- Addressed for the first time to one of the PICARO program consultations at the University Hospital of Caen Normandy,

- Written informed consent,

- Patient beneficiary of the french social insurance.

Exclusion Criteria:

- Minor and major protected patients

- pregnant or nursing women

- patient already included in the PICARO cohort

- Patients under guardianship, curatorship, safeguard of justice or legal protection.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
observational cohort with plasma samples
plasma samples

Locations

Country Name City State
France CHU Caen Caen Normandy

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With AntiCancer Drugs-Related Cardiac Adverse Events during the follow-up 2 years
Secondary Plasmatic tests to predict anticancer drugs-related cardiac adverse events from the constitution of the plasma biobank 2 years
See also
  Status Clinical Trial Phase
Not yet recruiting NCT06309862 - Immune Checkpoint Inhibitor Therapy for Cancer and Risk of Myocarditis or Cardiomyopathy
Recruiting NCT06302634 - Cardio-Oncology Rehabilitation Care Process
Recruiting NCT05150080 - Early Identification and Evaluation of Cyclophosphamide Cardiotoxicity