Clinical Cohorts in Coronary Disease Collaboration

NCT02402478 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3345

Last updated 2015-03-30

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02402478 on ClinicalTrials.gov