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Clinical Trials/NCT02388893
NCT02388893
Unknown
Not Applicable

Endocarditis Registry of the University Hospital of Cologne (ER-UHC)

University of Cologne1 site in 1 country500 target enrollmentStarted: January 2013Last updated:

Overview

Phase
Not Applicable
Enrollment
500
Locations
1
Primary Endpoint
All-cause mortality

Overview

Brief Summary

As recommended in the Guidelines on the prevention, diagnosis, and treatment of infective endocarditis (IE) patients with IE should be evaluated and managed by a multispecialty team including an cardiologist, infectious disease specialist, and cardiac surgeon. Our registry is a prospective, national registry of patients with IE. From January 2013 data from endocarditis board were prospectively recorded using standard definitions during the hospitalization. Patient demographics, clinical, laboratory, and imaging data at the time of IE diagnosis, as well as treatment outcomes were entered into the ER-UHC database.

Detailed Description

The primary endpoint will be the 1 year all-cause mortality after treatment begins of IE. We will use 1 year all-cause mortality as the primary endpoint because it has been demonstrated that a period of at least 6 months is necessary to offset the early postoperative mortality related to valve surgery. We also looked at all-cause in-hospital mortality as a secondary endpoint.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All patients with patients with definitive infective endocarditis

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

All-cause mortality

Time Frame: 1 year

1-year all-cause mortality

Secondary Outcomes

  • Inhospital all-cause mortality(1 month)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Guido Michels

Dr. Guido Michels

University of Cologne

Study Sites (1)

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