Clinical trial
A Phase II, International, Multi-centre, Prospective, Randomised, Parallel-group, Double-blind, Dose-ranging, Placebo-controlled, 12-week, Princeps Study to Assess the Efficacy and Safety of a One Injection Cycle With Either Botulinum Toxin Type-A (Dysport® 125, 250 or 500 Units) or Placebo Followed by an Optional 6-month Extension Phase in the Symptomatic Treatment of Micturition Urgency and Frequency in Continent Female Subjects Suffering From Idiopathic Overactive Bladder.
NCT00578097 is registered in ClinicalTrials.gov with Ipsen as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase II, International, Multi-centre, Prospective, Randomised, Parallel-group, Double-blind, Dose-ranging, Placebo-controlled, 12-week, Princeps Study to Assess the Efficacy and Safety of a One Injection Cycle With Either Botulinum Toxin Type-A (Dysport® 125, 250 or 500 Units) or Placebo Followed by an Optional 6-month Extension Phase in the Symptomatic Treatment of Micturition Urgency and Frequency in Continent Female Subjects Suffering From Idiopathic Overactive Bladder.
- Lead sponsor
- Ipsen
- Phase
- Phase 2
- Overall status
- Terminated
- Start date
- February 29, 2008
- Completion date
- December 31, 2009
- Enrollment
- 81 (actual)
- Sites
- 34
Conditions
As the registry lists them; a condition with its own page is linked.
overactive bladder