Study of Efficacy & Safety for 3 Infusion Regimens of IV Conivaptan in Subjects With Euvolemic or Hypervolemic Hyponatremia
Completed · Phase 3 · Has a placebo group
Conditions studied: Hyponatremia
In brief
The study is designed to assess the efficacy and safety of multiple infusions of conivaptan in subjects with euvolemic or hypervolemic hyponatremia
Key facts
- Study ID
- NCT00478192
- Run by
- Cumberland Pharmaceuticals
- People needed
- 50
- Starts
- 2007-04-01
- Expected to finish
- 2008-08-01
- Last updated by the study team
- 2014-05-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Euvolemic or hypervolemic (edematous) based on clinical presentation
- Serum sodium between 115 and 130mEq/L at baseline
You may not qualify if…
- Clinical presentation of volume depletion or dehydration
Where it is running
- Study site — Huntsville, Alabama, United States
- Study site — Tucson, Arizona, United States
- Study site — Los Angeles, California, United States
- Study site — Denver, Colorado, United States
- Study site — Jacksonville, Florida, United States
- Study site — Port Charlotte, Florida, United States
- Study site — Chicago, Illinois, United States
- Study site — Indianapolis, Indiana, United States
- Study site — Hazard, Kentucky, United States
- Study site — Detroit, Michigan, United States
- Study site — Omaha, Nebraska, United States
- Study site — The Bronx, New York, United States
- Study site — Cincinnati, Ohio, United States
- Study site — Fairfield, Ohio, United States
- Study site — Toledo, Ohio, United States
- Study site — Philadelphia, Pennsylvania, United States
- Study site — Philadelphia, Pennsylvania, United States
- Study site — Philadelphia, Pennsylvania, United States
- Study site — Philadelphia, Pennsylvania, United States
- Study site — Charleston, South Carolina, United States
- Study site — Orangeburg, South Carolina, United States
- Study site — Coimbatore, India
- Study site — Indore, India
- Study site — Jaipur, India
- Study site — Karnāl, India
Full record on ClinicalTrials.gov
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