Drug Wastage : Observational Study in Intensive Care Units in France
Launched by CENTRE HOSPITALIER INTERCOMMUNAL DE TOULON LA SEYNE SUR MER · Sep 21, 2022
Trial Information
Current as of July 09, 2025
Completed
Keywords
ClinConnect Summary
Observational study with data collection during a 24-hour business day. Data collected refer to healthcare team's practices and patients.
Collection starts when day shift starts (at 7:00 am) and ends when night shift leaves (at 7:00 am the following day).
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Adult patients hospitalized in intensive care units during the 24 hours of data collection.
- Exclusion Criteria:
- • Patient's opposition to participate in the study or patient family opposition if the patient is not able to be informed.
About Centre Hospitalier Intercommunal De Toulon La Seyne Sur Mer
The Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer is a leading healthcare institution dedicated to providing high-quality medical care and advancing clinical research. Located in the Provence-Alpes-Côte d'Azur region of France, this hospital collaborates with various healthcare professionals and research organizations to conduct innovative clinical trials aimed at improving patient outcomes. With a commitment to excellence in patient care and a multidisciplinary approach to research, the Centre Hospitalier Intercommunal plays a pivotal role in addressing healthcare challenges and contributing to the development of new therapeutic options in the medical field.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Bron, , France
Paris, , France
Limoges, , France
Paris, , France
Lyon, , France
Marseille, , France
Lyon, , France
Clermont Ferrand, , France
Paris, , France
Monaco, , Monaco
Brest, , France
Paris, , France
La Tronche, , France
Toulouse, Haute Garonne, France
Lyon, Rhône, France
Poitiers, Vienne, France
Reims, Marne, France
Brest, , France
Saint Pierre, , France
Mamoudzou, , Mayotte
Toulon, Var, France
Brest, Finistère, France
Toulon, Var, France
Lyon, Rhône, France
Bron, Rhône, France
Toulon, Var, France
Charleville Mézières, Ardennes, France
Strasbourg, Bas Rhin, France
Marseille, Bouches Du Rhône, France
Aurillac, Cantal, France
La Rochelle, Charente Maritime, France
Besançon, Doubs, France
Montélimar, Drôme, France
Quincy Sous Sénart, Essonne, France
Brest, Finistère, France
Nîmes, Gard, France
Bordeaux, Gironde, France
Bordeaux, Gironde, France
Libourne, Gironde, France
Pessac, Gironde, France
Quint Fonsegrives, Haute Garonne, France
Toulouse, Haute Garonne, France
Toulouse, Haute Garonne, France
Le Puy En Velay, Haute Loire, France
Antony, Hauts De Seine, France
Clamart, Hauts De Seine, France
Neuilly Sur Seine, Hauts De Seine, France
Rennes, Ille Et Vilaine, France
Chambray Lès Tours, Indre Et Loire, France
La Tronche, Isère, France
Dax, Landes, France
Mont De Marsan, Landes, France
Blois, Loir Et Cher, France
Saint Nazaire, Loire Atlantique, France
Orléans, Loiret, France
Montbrison, Loire, France
Saint Priest En Jarez, Loire, France
Cahors, Lot, France
Angers, Maine Et Loire, France
Saint Lô, Manche, France
Mamoudzou, Mayotte, France
Vannes, Morbihan, France
Nevers, Nièvre, France
Lille, Nord, France
Lille, Nord, France
Clermont Ferrand, Puy De Dôme, France
Saint Denis, Réunion, France
Saint Pierre, Réunion, France
Meaux, Seine Et Marne, France
Amiens, Somme, France
Trévenans, Territoire De Belfort, France
Argenteuil, Val D'oise, France
Créteil, Val De Marne, France
Le Chesnay, Yvelines, France
Bordeaux, Gironde, France
Montélimar, , France
Saint Denis, , France
Patients applied
Trial Officials
Erwan D'ARANDA, MD
Study Director
Sainte-Anne Military Teaching Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials