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Recruiting Not applicable

Evolution of PET Fixation With FDG at the End of Antibiotic Treatment of Infective Endocarditis on Valvular Prosthesis

NCT05989152 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-04-17
Last updated
2025-08-05

Condition(s) studied

Prosthetic Valve Endocarditis

Investigational drug(s) / intervention(s)

FDG-PET at the end of treatment for IE

FDG-PET at the end of treatment for IE: FDG-PET at the end of treatment for IE in patients with a prosthetic valve

Study summary

In patients with prosthetic valve endocarditis (PVE) and pathological valvular FDG uptake on the initial FDG-PET and not referred to valve replacement at the acute phase, the study will assess whether FDG-PET is able to identify those at increased risk of PVE relapse.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
"Inclusion criteria: * Patient aged 18 or over; * Have a prosthetic valve implanted surgically or by catheter for at least 3 months; * Presenting a definite IE on a prosthetic valve (ESC definition in force); * Having benefited from an FDG-PET examination for diagnostic purposes as part of the treatment revealing pathological hyperuptake at the level of the prosthetic valve AND carried out \<15 days after the start of antibiotic therapy for infective endocarditis; * Absence of cardiac surgical intervention performed for the current episode of AE or planned before the end-of-treatment FDG-PET Exclusion criteria: * Patient under legal protection, guardianship or curators; * Pregnancy, breastfeeding; * Patient not affiliated to a health insurance scheme or not a beneficiary of a social security scheme; * Simultaneous participation in a study on FDG-PET; * Absence of informed consent signed by the patient."

Primary outcome measure(s)

  • Presence of pathological uptake on the prosthetic valve on FDG-PET — at inclusion
    Presence of pathological uptake on the prosthetic valve on FDG-PET performed after the recommended duration of curative antibiotic treatment

Trial sites (1)

FacilityCityRegionStatus
Hôpital Bichat-Claude Bernard Paris France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05989152 on ClinicalTrials.gov ↗ ← All trials in France