Clinical trial

An 8 Week Study Looking At The Efficacy, Toleration And Safety Of SS-RBX For…

NCT00138749 · Pfizer, Industry · Completed

Key facts

NCT number NCT00138749
Title An 8 Week Study Looking At The Efficacy, Toleration And Safety Of SS-RBX For Stress Urinary Incontinence.
Official title An 8-Week, Multi-Centre,Randomised Double-Blind, Placebo Controlled, Parallel Group Study To Evaluate The Efficacy,Toleration And Safety Of (+)- [S,S]- Reboxetine In The Treatment Of Stress Urinary Incontinence (SUI) In Women.
Lead sponsor Pfizer, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Urinary Incontinence, Stress
Intervention type Drug
Interventions SS-RBX
Enrollment 402
Start date Nov 1, 2004
Primary completion Aug 1, 2006
Completion Aug 1, 2006
First posted Aug 30, 2005
Last update posted Apr 7, 2011
Countries Canada, United States

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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