Adult Congenital Heart Disease Registry (QuERI)

Status Completed

Clinical Trial Summary

Multi-center, observational, U.S.-based longitudinal program. Data will be collected prospectively for 3 years. Individual physician feedback will be provided on data collected with the purpose of improving the management of patients - quality enhancement research initiative (QuERI) process from adult patients enrolled with a history of repaired Congenital Heart Disease (CHD).

Clinical Trial Description

Approximately 800 male and female adult patients with a history of repaired CHD will be recruited from approximately 100 cardiology practices and will be followed up every twelve months for the period of three years. Consecutive patients in each practice meeting inclusion and exclusion criteria should be considered for the study. Two groups of subjects will be enrolled based on identical exclusion criteria and inclusion criteria, with the exception only of inclusion criteria #3: cohort 1- those demonstrating historic high risk criteria and cohort 2 - those demonstrating current high risk criteria. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01659411
Study type	Observational [Patient Registry]
Source	Actelion
Contact
Status	Completed
Phase
Start date	December 1, 2011
Completion date	May 16, 2018

View Details

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