Status: Not yet recruiting
Canadian Adult Congenital Heart Disease Intervention Registry
The ACHDi Registry study will create a foundational database for adult congenital heart disease interventions. This Pan-Canadian Registry will collect clinical and patient-reported information that will enable the evaluation of care processes and outcomes in five most common ACHDi interventions by enabling prospective and retrospective registry-based studies to answer important clinical practice and policy-relevant questions.
Participants needed: 9,000
Trial details
Age: 18-110Biological sex: AllType: ObservationalSponsor: University Health Network, TorontoUpdated: Feb 28, 2020Locations: 1Duration: 10 Years
Eligibility criteria
participants must be 18 years or older referred for intervention for one of five...
participants below the age of 18 [+1]