dbGaP Protocol: The Pediatric Cardiac Genetics Consortium (PCGC)

Completed

Conditions studied: Congenital Heart Disease

In brief

Background: Researchers do not know much about the causes of congenital heart disease (CHD). They do know that many factors play a role. Some factors are environmental. Some are genetic. But few specific factors have been identified. And researchers do not know how many involve genes. They want to study data that has already been collected from people with CHD and their families. Objectives: To identify genetic variations related to CHD. To study molecules related to vascular disease in order to learn new ways to treat it. Eligibility: People who already participated in the Pediatric Cardiac Genomics Consortium (PCGC) study Design: Researchers will study data that was already collected in the PCGC. There will be no active participants. Researchers will get access to the data through the coordinating center. They will not download data to local storage devices. The data will have no personally identifying information....

Key facts

Study ID
NCT03347214
Run by
National Heart, Lung, and Blood Institute (NHLBI)
People needed
6260
Starts
2017-10-20
Expected to finish
2020-01-10
Last updated by the study team
2020-01-18

Who can join

Age: any, up to 60. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.