Viewing Study NCT00281567



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Study NCT ID: NCT00281567
Status: COMPLETED
Last Update Posted: 2013-11-01
First Post: 2006-01-24

Brief Title: Efficacy and Safety Comparison of Tiotropium Inhalation Solution Respimat Inhaler and Spiriva HandiHaler in Chronic Obstructive Pulmonary Disease COPD
Sponsor: Boehringer Ingelheim
Organization: Boehringer Ingelheim

Study Overview

Official Title: A Randomised Double-blind Double-dummy Placebo-controlled Crossover Efficacy and Safety Comparison of 4-week Treatment Periods of Two Doses 5 μg 2 Actuations of 25 μg and 10 μg 2 Actuations of 5 μg of Tiotropium Inhalation Solution Delivered by the Respimat Inhaler Tiotropium Inhalation Powder Capsule 18μg Delivered by the HandiHaler in Patients With Chronic Obstructive Pulmonary Disease COPD
Status: COMPLETED
Status Verified Date: 2013-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Comparison of lung function response between tiotropium inhalation solution and Spiriva HandiHaler
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None