drugset / Trial / NCT00478192
Study of Efficacy & Safety for 3 Infusion Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia
RandomizedParallel-groupDouble-blindTreatment
Summary
The study is designed to assess the efficacy and safety of multiple infusions of conivaptan in subjects with euvolemic or hypervolemic hyponatremia
Timeline
- Start
- 2007-04
- Primary completion
- 2008-08
- Completion
- 2008-08
Outcome
Met primary endpoint
registry Regimen 1 Conivaptan QD vs Regimen 3 Placebo; p = 0.019; ANCOVA NCT00478192 ↗
registry Regimen 2 Conivaptan BID vs Regimen 3 Placebo; p <0.001; ANCOVA NCT00478192 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Conivaptan | Small molecule | 20 mg | Intravenous |
Indications
No indication recorded.