Prospective Cohort Study of Patients With Infective Endocarditis at Pitié-Salpêtrière Hospital

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Infective endocarditis (IE) is a severe condition associated with high mortality. Due to the relative low prevalence of IE, prospective data are lacking and current guidelines are mostly based on expert consensus with low level of evidence. IE is also associated with severe complications especially strokes that occur in about one third of the patients.

In order to improve the management and the prognosis of IE, clinical data from larges prospective cohort studies are needed.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with confirmed IE according to European Society of Cardiology criteria

Disqualifiers

Opposition of the patient to participate

Trial population

All the patients with IE admitted at Cardiology institute of the Pitié-Salpêtrière hospital

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

All-cause in hospital mortality

All-cause mortality during the length of hospital stay

Time frame
up to 90 days

Secondary outcomes

1

All-cause mortality

mortality at longest follow-up

Time frame
an average of 10 years
2

symptomatic or asymptomatic systemic embolism

symptomatic or asymptomatic systemic embolism confirmed by any type of imaging during initial hospitalization

Time frame
up to 90 days after inclusion
3

Association between coagulation biomarkers (D-dimer, fibrin monomer, circulating anticoagulant, von Willebrandt factor (VWF) antigen level, von Willebrandt factor (VWF) activity) assessed at the inclusion and the presence of systemic embolism

Association between coagulation biomarkers (D-dimer, fibrin monomer, circulating anticoagulant, von Willebrandt factor (VWF) antigen level, von Willebrandt factor (VWF) activity) assessed at the inclusion and the presence of systemic embolism at the admission Initial Hospitalization

Time frame
inclusion
4

Association between coagulation biomarkers (D-dimer, fibrin monomer, circulating anticoagulant, von Willebrandt factor (VWF) antigen level, von Willebrandt factor (VWF) activity) assessed at the inclusion and the presence of systemic embolism

Association between coagulation biomarkers(D-dimer, fibrin monomer, circulating anticoagulant, von Willebrandt factor (VWF) antigen level, von Willebrandt factor (VWF) activity) assessed at the inclusion and the presence of systemic embolism within 90 days after admission

Time frame
up to 90 days after inclusion

Other outcomes

Sponsors and contacts

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