Assessing treatments for difficult-to-treat Pseudomonas infections
Antimicrobial Therapy for Infections Due to Pseudomonas Aeruginosa With Difficult-to-treat Resistance: a Real-world, Prospective, Multicenter Cohort Study
This study is testing different antibiotic treatments for tough Pseudomonas infections to see which ones work best for patients needing intravenous therapy.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 600 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Régional d'Orléans Academic / other |
| Locations | 48 sites (Amiens and 47 other locations) |
| Trial ID | NCT06738771 on ClinicalTrials.gov |
What this trial studies
The ADDICT study aims to evaluate the clinical efficacy of various antimicrobial therapies for infections caused by difficult-to-treat Pseudomonas aeruginosa. This prospective, multicenter cohort study will include patients requiring intravenous therapy for these infections, comparing newer beta-lactam/beta-lactamase inhibitor combinations and cefiderocol against older agents like aminoglycosides and colistin. The study will also investigate the emergence of drug resistance and the associated adverse events. By gathering multicenter data, the study seeks to provide insights into the real-life effectiveness of these treatment options.
Who should consider this trial
Good fit: Ideal candidates are patients aged 18 or older who require intravenous antimicrobial therapy for a difficult-to-treat Pseudomonas aeruginosa infection.
Not a fit: Patients with cystic fibrosis or those who do not require definitive intravenous antibiotic therapy for their Pseudomonas infection may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment options for patients with difficult-to-treat Pseudomonas infections.
How similar studies have performed: While there is limited multicenter data on the real-life utilization of these treatment options, previous studies have shown promising results with similar approaches.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All patients aged 18 or over and requiring intravenous definite antimicrobial therapy for a DTR P. aeruginosa infection Exclusion Criteria: * Cystic fibrosis * P. aeruginosa DTR colonization or P. aeruginosa DTR infection not requiring definitive intravenous antibiotic therapy * Protected person (under guardianship or curatorship) * Persons under court protection * Persons deprived of liberty * Opposition expressed for participation in the study
Where this trial is running
Amiens and 47 other locations
- CHU Amiens — Amiens, France (Not_yet_recruiting)
- CH Argenteuil — Argenteuil, France (Not_yet_recruiting)
- CH Bayonne — Bayonne, France (Not_yet_recruiting)
- CHU de BESANCON — Besançon, France (Not_yet_recruiting)
- CH Bethune — Béthune, France (Not_yet_recruiting)
- CHU Avicenne — Bobigny, France (Not_yet_recruiting)
- CH Bourgoin-Jallieu — Bourgoin, France (Not_yet_recruiting)
- CH Métropole Savoie — Chambéry, France (Not_yet_recruiting)
- Ch de Chartres — Chartres, France (Not_yet_recruiting)
- CHU Clermont Ferrand — Clermont-Ferrand, France (Not_yet_recruiting)
- CHI Créteil — Créteil, France (Not_yet_recruiting)
- CHU Henri Mondor — Créteil, France (Not_yet_recruiting)
- CHI Elbeuf Louviers — Elbeuf, France (Not_yet_recruiting)
- CH Sud Essone — Étampes, France (Not_yet_recruiting)
- Hopital Raymond Poincaré — Garches, France (Not_yet_recruiting)
- CHU Grenoble — Grenoble, France (Not_yet_recruiting)
- CH Haguenau — Haguenau, France (Not_yet_recruiting)
- CHD Vendée — La Roche-sur-Yon, France (Recruiting)
- Hopital Bicetre — Le Kremlin-Bicêtre, France (Not_yet_recruiting)
- CHU Limoges — Limoges, France (Not_yet_recruiting)
- CHU Lyon Sud — Lyon, France (Not_yet_recruiting)
- CHU Lyon — Lyon, France (Not_yet_recruiting)
- CHY Lyon — Lyon, France (Not_yet_recruiting)
- Hopital Saint-Joseph Saint Luc — Lyon, France (Not_yet_recruiting)
- CHU Montpellier — Montpellier, France (Not_yet_recruiting)
- CHRU Nancy — Nancy, France (Recruiting)
- Chu de Nantes — Nantes, France (Not_yet_recruiting)
- CHU de Nice — Nice, France (Not_yet_recruiting)
- Centre Hospitalier Universitaire d'Orléans — Orléans, France (Recruiting)
- Hopital Bichat — Paris, France (Recruiting)
- Hopital Cochin — Paris, France (Not_yet_recruiting)
- Hopital LARIBOISIERE — Paris, France (Not_yet_recruiting)
- Hopital Pitie Salpetriere — Paris, France (Not_yet_recruiting)
- Hopital Saint-Antoine — Paris, France (Not_yet_recruiting)
- Hôpital Européen Georges Pompidou — Paris, France (Not_yet_recruiting)
- Hôpital Saint-Louis — Paris, France (Not_yet_recruiting)
- Ch Pau — Pau, France (Not_yet_recruiting)
- CH Perpignan — Perpignan, France (Not_yet_recruiting)
- Centre Hospitalier de Périgueux — Périgueux, France (Not_yet_recruiting)
- CHU Reims — Reims, France (Not_yet_recruiting)
- CH Saint-Lô — Saint-Lô, France (Not_yet_recruiting)
- CHRU Strasbourg Haute Pierre — Strasbourg, France (Not_yet_recruiting)
- CHU Strasbourg — Strasbourg, France (Not_yet_recruiting)
- Hopital Foch — Suresnes, France (Not_yet_recruiting)
- CH Tourcoing — Tourcoing, France (Not_yet_recruiting)
- CH Vannes — Vannes, France (Not_yet_recruiting)
- Hôpital Nord-Ouest de Villefranche sur Saone — Villefranche-sur-Saône, France (Not_yet_recruiting)
- CHU La Réunion — Saint-Denis, Reunion (Not_yet_recruiting)
Study contacts
- Principal investigator: Francois BARBIER, Professor — Centre Hospitalier Universitaire d'Orléans
- Study coordinator: FRANCOIS BARBIER, Professor
- Email: francois.barbier@chu-orleans.fr
- Phone: +33238229939
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.