RecruitingPhase 3NCT07345325

Rifampin-free Regimen Versus Rifampin-containing Regimen in the Treatment of Staphylococcal Prosthetic Valve Endocarditis

Rifampin-free Regimen Versus Rifampin-containing Regimen in the Treatment of Staphylococcal Prosthetic Valve Endocarditis: a Multicenter Randomized Controlled Non-inferiority Study


Sponsor

Nantes University Hospital

Enrollment

422 participants

Start Date

Jun 11, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The primary objective of this study is to demonstrate that a rifampin-free regimen is non-inferior to the rifampin-containing regimen in terms of all-cause mortality in staphylococcal prosthetic valve endocarditis within 6 months after randomization.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Rifampin containing regimen and a drug called Rifampin-free regimen for people with infective endocarditis. The study is currently recruiting participants at 31 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRifampin-free regimen

Rifampin-free regimen. The choice of other antibiotics is at the discretion of the physicians in charge but should be in accordance with the 2023 ESC guidelines and 2025 French guidelines (AEPEI/SPILF).

DRUGRifampin containing regimen

Rifampin containing regimen (900 mg/day). Antibiotic treatment of endocarditis in accordance with the 2023 ESC guidelines and 2025 French guidelines.


Locations(31)

CH metropole Savoie, Chambery, GHT Savoie-Belley, Site Aix les Bains

Aix-les-Bains, France

CHU Angers

Angers, France

CHU Besançon

Besançon, France

CHU Bordeaux, Cardiologic hospital of Haut lévêque

Bordeaux, France

CHU Bordeaux, Haut Lévêque Hospital, Infectious disease department

Bordeaux, France

CHU Brest

Brest, France

AP-HP, Groupe hospitalier Henri Mondor

Créteil, France

CHU Dijon Bourgogne

Dijon, France

CHU Grenoble

Grenoble, France

CHD Vendée

La Roche-sur-Yon, France

CHU Lyon, La Croix-Rousse Hospital, Infective disease department

Lyon, France

CHU Lyon, Louis Pradel Hospital, Cardiology Institute

Lyon, France

CHU Montpellier

Montpellier, France

CHU Nancy

Nancy, France

CHU Nantes, Hôtel Dieu Hospital, Infective disease department

Nantes, France

CHU Nantes, Laennec Hospital, Cardiology department

Nantes, France

CHU Nice

Nice, France

CHR Orléans

Orléans, France

AP-HP hôpital St Antoine

Paris, France

AP-HP, Hôpital Pitié Salpétrière

Paris, France

AP-HP, hôpital Bichat-Claude Bernard

Paris, France

CH Pau

Pau, France

CHU Poitiers

Poitiers, France

CH intercommunal Cornouaille Quimper

Quimper, France

CHU Rennes

Rennes, France

CHU St-Etienne

Saint-Etienne, France

CHU Strasbourg

Strasbourg, France

CHU Toulouse, Purpan Hospital, Infectious disease department

Toulouse, France

CHU Toulouse, Rangueil Hospital, Cardiology department

Toulouse, France

CH Tourcoing

Tourcoing, France

CHU Tours

Tours, France

View Full Details on ClinicalTrials.gov

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NCT07345325


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