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Design studies of nebulization in COPD does not respond adequately to the clinically relevant question: the intervention of administering nebulized bronchodilators at home it is likely to make a profit, compared to the standard optimized treatment as defined by the recommendations of the SPLF, patients with severe COPD (stage III, FEV between 30% and 50% of the theoretical value) and very severe (stage IV, less than 30% of the theoretical value FEV)? The concept of profit in this context is based on criteria of dyspnea, quality of life, use of health system (exacerbations, hospitalizations, prescription of antibiotics and steroids ...).
Age
18 - 80 years
Sex
ALL
Healthy Volunteers
No
Service de Pneumologie
Amiens, France
Service de Pneumologie
Angers, France
Service de Pneumologie
Brest, France
Service de Pneumologie
Grenoble, France
Service de Pneumologie
Limoges, France
Service de Pneumologie
Nancy, France
Service de Pneumologie
Nantes, France
Service de Pneumologie
Orléans, France
Service de Pneumologie
Paris, France
Service de Pneumologie
Poitiers, France
Start Date
January 1, 2012
Primary Completion Date
December 1, 2015
Completion Date
December 1, 2015
Last Updated
April 27, 2016
45
ACTUAL participants
Atrovent + Bricanyl or Atrovent + Ventoline
DRUG
Placebo
DRUG
Lead Sponsor
University Hospital, Tours
NCT05222295
NCT02138916
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT01854008