Viewing Study NCT00453778



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Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00453778
Status: COMPLETED
Last Update Posted: 2013-02-12
First Post: 2007-03-27

Brief Title: A Study To Investigate The Effect Of Inhaled Fluticasone Propionate On The Bronchial Responsiveness To Leukotriene D4 In Asthmatics Patients
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: A Study to Investigate the Effect of Inhaled Fluticasone Propionate on the Bronchial Responsiveness to Leukotriene D4 in Asthmatics Patients
Status: COMPLETED
Status Verified Date: 2013-02
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: Investigate if asthmatics treated with FLIXOTIDE FP 500 mcg BID during 14 days get reduced bronchial reactivity after inhalation of Leukotriene D4 Two 14 days treatment periods where patients received FP 500 MCG BID and placebo Washout at least 21 days between treatments Bronchial challenge with methacholine and Leukotriene D4 were performed before the start of each treatment period and on treatment days 13 and 14 respectively
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