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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00524212
Other study ID # 06-10-B640-A1205-22345
Secondary ID 20060181SUN-2007
Status Completed
Phase N/A
First received August 31, 2007
Last updated January 19, 2010
Start date March 2007
Est. completion date May 2009

Study information

Verified date January 2010
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics CommitteeDenmark: Danish Dataprotection Agency
Study type Observational

Clinical Trial Summary

The purpose is to exam prospective if simple clinical information in combination with a normal s-procalcitonin are sufficient for exclusion of infective endocarditis (IE).


Description:

Despite progress in surgical and medical treatment, infective endocarditis is still associated with high morbidity and mortality.

The variable clinical presentation of IE makes the diagnosis a clinical challenge.

Procalcitonin is a precursor from the hormone calcitonin and also a marker of systemic bacterial infections.

The purpose of this study is:

- to investigate the diagnostic value of serum procalcitonin (PCT), C-reactive protein (CRP) and sedimentation rate (SR) when IE is suspected.

- to investigate if a retrospectively generated clinical model suitable for exclusion of IE can be confirmed prospectively.


Recruitment information / eligibility

Status Completed
Enrollment 761
Est. completion date May 2009
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients > or = 18 year with suspected or verified Infective Endocarditis

- By word of mouth or in writing consent

Exclusion Criteria:

- Incapacity

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Department of Cardiology, Aarhus University Hospital Aarhus

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

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