drugset / Trial / NCT01684800
Comparative Trial to Investigate the Efficacy and Safety of Desmopressin for the Treatment of Nocturia in Adult Women
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of the study is to investigate the efficacy and safety of two different dose levels of desmopressin orally disintegrating tablets against placebo for the treatment of nocturia in adult women during 12 weeks treatment
Timeline
- Start
- 2012-09
- Primary completion
- 2013-06
- Completion
- 2013-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Desmopressin | Peptide | 10 ug | Oral |
| Comparator | Desmopressin | Peptide | 25 ug | Oral |