Viewing Study NCT00138749



Ignite Creation Date: 2024-05-05 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 9:13 AM
Study NCT ID: NCT00138749
Status: COMPLETED
Last Update Posted: 2011-04-07
First Post: 2005-08-26

Brief Title: An 8 Week Study Looking At The Efficacy Toleration And Safety Of SS-RBX For Stress Urinary Incontinence
Sponsor: Pfizer
Organization: Pfizer

Study Overview

Official Title: An 8-Week Multi-CentreRandomised Double-Blind Placebo Controlled Parallel Group Study To Evaluate The EfficacyToleration And Safety Of - SS- Reboxetine In The Treatment Of Stress Urinary Incontinence SUI In Women
Status: COMPLETED
Status Verified Date: 2011-04
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: A study designed to assess the efficacy toleration and safety of SS-RBX for the treatment of stress urinary incontinence
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