CHRU
Vandœuvre-lès-Nancy, 54511, France
Location status: Recruiting
NCT Number: NCT03272724
The objective of this observatory is to provide a national database of infective endocarditis, informed by all volunteer centers, using a standardized case report forms.
Such an observatory will describe the clinical profile, microbiological, therapeutic and evolving of infective endocarditis (IE); analyze the risk factors for the disease and its prognosis factors of evolution; describe management practices; evaluate and compare in the real drug treatment strategies (including antibiotics) and surgical.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Vandœuvre-lès-Nancy, 54511, France
Location status: Recruiting
All the clinical, biological, microbiological and laboratory describing the history of patients and their evolution during hospitalization for infective endocarditis will be obtained from physicians supporting patients and recorded in an electronic case report form. Will include collected clinical characteristics (site, pre-existing heart disease underlying symptoms, complications), biological characteristics (dosage on admission and diagnosis), microbiological characteristics (identifying the genus and species of the microorganism responsible, sensitivity to antibiotics susceptibility testing and evaluated by determination of minimal inhibiting concentration (MIC), exhaustive search of the rare forms of endocarditis uncultivated microorganisms), an analysis of the gateways based on the causative organism; echocardiographic characteristics (number and size of vegetations, valvular damage, scalable: surgery, lethality) and therapeutic characteristics (antibiotic treatment, surgical).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: inclusion
status of heart valves, pre-existing heart conditions
Time frame: inclusion
associated diseases
Time frame: period of 3 months before infective endocarditis
high risk procedures
Time frame: inclusion
kg
Time frame: inclusion
cm
Time frame: inclusion
cardiac, peripheral and neurological symptoms
Time frame: inclusion
blood count
Time frame: inclusion
identification of infecting organisms
Time frame: inclusion
description of tyhe imaging tests performed
Time frame: from inclusion to recovery
antibiotic treatment: type and duration
Time frame: from inclusion to recovery
description of surgical procedures
Time frame: inclusion
plasma and serum collection
Contact information is provided by the study sponsor or research team.
Central Hospital, Nancy, France
Other
Acronym: ObservatoireEI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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