drugset / Trial / NCT00478192

Study of Efficacy & Safety for 3 Infusion Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia

NCT00478192

Phase 3 Completed 50 enrolled Cumberland Pharmaceuticals
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

Drugs

EvaluationDrugModalityDoseRoute
Subject Conivaptan Small molecule 20 mg Intravenous

Indications

No indication recorded.