Endocarditis Clinical Trial
— NATIVTEPOfficial title:
Contribution of 18F-FDG PET-CT in the Diagnosis and the Detection of Peripheral Emboli of Infectious Endocarditis on Native Valves
Verified date | October 2020 |
Source | University Hospital, Bordeaux |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The diagnosis of infectious endocarditis is not always easy and is based on several clinical and imaging arguments. Positron Emission Tomography - Computed Tomography (PET-CT) has been validated for endocarditis on prosthetic valves but few studies concern the native valves. The purpose of the study is to estimate the diagnostic sensitivity of [18F]-fluoro-2-deoxyglucose (18F-FDG) PET-CT in patients with endocarditis on native valves according to the European Society of Cardiology 2015 (ESC 2015) modified diagnostic criteria of infective endocarditis classified as definite at three months of follow-up (baseline test).
Status | Completed |
Enrollment | 31 |
Est. completion date | September 16, 2020 |
Est. primary completion date | September 16, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Any patient = 18 years treated at the university hospital center of Bordeaux for suspicion of infectious endocarditis on a native valve with a "definite" or "possible" diagnosis according to the ESC 2015 modified diagnostic criteria, agreeing to participate, - Affiliated person or beneficiary of a social security scheme, - Free, informed and written consent (no later than the day of inclusion and before any exam required by the research). Exclusion Criteria: - Patient with a vital failure (haemodynamic, respiratory or neurological instability), requiring treatment in the intensive care unit and / or urgent surgery incompatible with performing PET-CT, - Pregnant or nursing woman, - Patient who has already been treated for infective endocarditis within six months of enrollment, - Patient who had cardiac surgery in the two months preceding inclusion, - Patient who has previously been hypersensitive to fluorodeoxyglucose and / or excipients of the radiotracer, - Patient unable to sign consent, - Patient under legal protection, - Women of childbearing age who do not benefit from effective contraception (HAS criteria), - Patient in a period of relative exclusion from another research protocol. |
Country | Name | City | State |
---|---|---|---|
France | University hospital, Bordeaux | Pessac |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Bordeaux |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Sensitivity of the 18F-FDG PET-CT in the diagnosis of infectious endocarditis | The reference test in this study will be a "definite diagnosis" of infectious endocarditis according to the ESC 2015 modified criteria at three months of follow-up, evaluated by a multidisciplinary committee in infectious endocarditis. This evaluation will be done blind to the results of the PET-CT of the study. The index test 18F-FDG PET-CT will have been performed at the initial phase of patient management. | 3 month |
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