Clinical Cohorts in Coronary Disease Collaboration
NCT02402478 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3345
Last updated 2015-03-30
Summary
The purpose of this study is to advance research through collaboration, 4C was established in the United Kingdom (UK) in 2009 as a resource in which deoxyribonucleic acid (DNA) and biomarker samples were obtained at time of presentation with chest pain linked to detailed phenotypic data obtained from electronic health records and participant self-completed questionnaires. The investigators sought to explore and assess the current potential of setting up a comparable consented research platform by collecting DNA samples and to quantify the extent to which diverse NHS hospital information systems are accessible for extracting secondary care data (structured and unstructured) for research purposes at scale.
Conditions
Sponsors & Collaborators
-
Barts & The London NHS Trust
collaborator OTHER -
University of Bristol
collaborator OTHER -
University of York
collaborator OTHER -
University College, London
lead OTHER
Principal Investigators
-
Harry Hemingway, Prof · Farr Institute of Health Informatics Research
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-07-31
- Primary Completion
- 2014-01-31
- Completion
- 2014-01-31
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