drugset / Trial / NCT02244281
Study of FLOMAX® Versus Placebo in Female Patients With Lower Urinary Tract Symptoms (LUTS) With a Significant Component of Voiding Symptoms
RandomizedParallel-groupDouble-blindTreatment
Summary
1. To study the symptomatic improvement in LUTS afforded by FLOMAX® capsules, 0.4 mg daily compared to placebo, in female patients with lower urinary tract symptoms (LUTS) with a significant component of voiding symptoms 2. To study the improvement afforded by FLOMAX® capsules versus placebo, in this patient population, in quality of life 3. To assess the safety and tolerability of FLOMAX® capsules, 0.4 mg compared to placebo, in women suffering from LUTS with a significant component of voiding symptoms
Timeline
- Start
- 2001-05
- Primary completion
- 2003-11
- Completion
- —
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tamsulosin | Other / unclassified | 0.4 mg | — |
Indications
No indication recorded.