drugset / Trial / NCT00435591

A Study of Multiple Dosing Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia

NCT00435591

Phase 4 Completed 121 enrolled Cumberland Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The study will evaluate the effectiveness and safety of multiple dosing regimens of IV conivaptan in subjects with euvolemic or hypervolemic hyponatremia

Timeline

Start
2007-01
Primary completion
2008-09
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Conivaptan Small molecule 20 mg Intravenous

Indications

No indication recorded.