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French National Registry of Patients With Tetralogy of Fallot and Implantable Cardioverter Defibrillator — DAI-T4F  

Congenital Heart Disease Clinical Trial

Official title:
French National Registry of Patients With Tetralogy of Fallot and Implantable Cardioverter Defibrillator

Clinical Trial Summary

National french registry of patients with tetralogy of Fallot and implantable cardioverter defibrillator.

Clinical Trial Description

Inclusion criteria:

- patient with tetralogy of Fallot > 18 years

- implantable cardioverter defibrillator (ICD)

- primary or secondary prevention

All french centers performing ICD implantation are annually contacted to include all patients with tetralogy of Fallot and ICD.

Retrospective inclusion of cases before 2010 and prospective inclusion after 2010 with prospective follow up and annual update.

All events are centrally adjudicated with collection of all baseline ECG and reviewing of endocavitary EGM. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03837574
Study type Observational [Patient Registry]
Source Paris Sudden Death Expertise Center
Contact Victor Waldmann, MD
Phone +33676098007
Email vicrtor.waldmann@inserm.fr
Status Recruiting
Phase
Start date December 1, 2010
Completion date December 31, 2030
View Details
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