Barts Endocarditis Research Registry
NCT06434012 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2025-07-15
Summary
The Barts Endocarditis Research Registry is being set up to give a unique opportunity to assess the characteristics of Infective Endocarditis (IE) in our population cohort, the current use of imaging techniques, as well as the implementation of the ESC guidelines and its consequence in terms of prognosis. All this will help improve the diagnosis and management of IE. The registry will also form the core of all our subsequent work, including interventional studies. The endocarditis research registry is to record the epidemiological, demographic, microbiological, surgical and outcome data in our cohort of endocarditis patients. This work will underpin all future work in endocarditis by clearly defining our patient cohort and the outcomes from treatment. We have a series of studies planned that we believe will influence the management of endocarditis (we are working up proposals for genomic and therapeutic trials that will subsequently be presented for ethical and hospital approval). The registry will be generic to all our planned studies, and will allow us to capture data to assess treatment effectiveness
Conditions
- Infective Endocarditis
- Endocarditis
- Endocarditis, Bacterial
Interventions
- OTHER
-
registry
This is registry for Infective Endocarditis
Sponsors & Collaborators
-
Queen Mary University of London
lead OTHER
Principal Investigators
-
Simon Woldman, MSc · St Bartholomews Hospital
Eligibility
- Min Age
- 16 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-04-24
- Primary Completion
- 2029-04-24
- Completion
- 2029-04-30
Countries
- United Kingdom
Study Locations
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