Ignite Creation Date:
2024-05-05 @ 5:25 PM
Last Modification Date:
2024-10-26 @ 9:31 AM
Study NCT ID:
NCT00446667
Status:
WITHDRAWN
Last Update Posted:
2016-09-28
First Post:
2007-03-12
Brief Title:
A Pilot Safety Study of Inhaled Dry Powder Mannitol in Acute Exacerbations of COPD
Sponsor:
Syntara
Organization:
Syntara
Study Overview
Official Title:
A Pilot Safety Study of Inhaled Dry Powder Mannitol in Acute Exacerbations of COPD
Status:
WITHDRAWN
Status Verified Date:
2016-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Failed to recruit
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
COPD is a major cause of ill health and death in Australia with 40000 hospital admissions and a national cost of 898000000 annually The gold standard treatment of COPD is steroids for inflammation antibiotics for infection and bronchodilators and oxygen for respiratory failure However associated mucus hypersecretion is responsible for much of the inflammation and infection The use of pharmaceutical agents to assist in the early clearance of the retained mucus has been limited primarily because of lack of demonstrated effect There has been a recent development of interest in pursuing new therapies for improving mucociliary clearance and several studies have demonstrated that clinical outcomes can be improved when osmotic agents such as mannitol are added to standard treatments The purpose of this study is to conduct a pilot safety study in patients with an acute exacerbation of COPD to determine if it is safe to administer inhaled mannitol for facilitating mucus clearance
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