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NCT00380575 · ClinicalTrials.gov registry record · Phase 3
Study of IV YM087 to Assess Efficacy and Safety in Patients With Euvolemic or Hypervolemic Hyponatremia
A Phase 3 study of Hyponatremia, sponsored by Cumberland Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 84
- Enrollment target
- 20
- Study locations
NCT00380575 is a Phase 3 study of Hyponatremia that has completed, run by Cumberland Pharmaceuticals. The registered enrollment target is 84 participants, below the 310-participant average among 3 other Hyponatremia trials with a reported enrollment target (73% lower). The trial reports 20 study locations across 15 states.
The verdict
NCT00380575, a Phase 3 study of Hyponatremia, has completed, sponsored by Cumberland Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 84 participants
- Enrollment target
- 20
- Study locations
Study Summary
This study will investigate the application of a vasopressin antagonist in the treatment of hyponatremia most likely caused by inappropriate AVP secretion. The population studied will include patients with euvolemic or hypervolemic hyponatremia.
Conditions Studied
Interventions
- DRUG YM087
Study Locations (20)
California
- - La Jolla
- - Los Angeles
- - Santa Rosa
Arizona
- - Phoenix
- - Tuscon
Florida
- - Miami
- - Plantation
Missouri
- - Rolla
- - St Louis
Alabama
- - Mobile
Illinois
- - Springfield
Indiana
- - Indianapolis
Louisiana
- - Shreveport
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 84 participants |
| Start Date | 2000-08 |
| Est. Completion | 2003-02 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00380575
The ClinicalTrials.gov registry entry for NCT00380575 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 84 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 310-participant average among 3 other Hyponatremia trials with a reported enrollment target (73% lower). The listed sponsor is Cumberland Pharmaceuticals, which has 43 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Hyponatremia appearing as the primary indexed condition, and to 1 intervention - of which YM087 is the first listed.
NCT00380575 reports 20 study locations spanning 15 distinct geographic areas - top geographies include California, Arizona, Florida.
Frequently Asked Questions
What is clinical trial NCT00380575 about?
NCT00380575 is a clinical study titled "Study of IV YM087 to Assess Efficacy and Safety in Patients With Euvolemic or Hypervolemic Hyponatremia". This study will investigate the application of a vasopressin antagonist in the treatment of hyponatremia most likely caused by inappropriate AVP secretion. The population studied will include patients with euvolemic or hypervolemic hyponatremia.
What is the current status of trial NCT00380575?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 84 participants. The study started on 2000-08. Estimated completion is 2003-02.
What conditions does trial NCT00380575 study?
This clinical trial studies the following conditions: Hyponatremia.
What interventions are being tested in trial NCT00380575?
The interventions under investigation include: YM087 (DRUG).
Who is sponsoring clinical trial NCT00380575?
This trial is sponsored by Cumberland Pharmaceuticals, which has 43 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00380575 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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An Open-Label Study of YM087 (Conivaptan) in Patients With Euvolemic or Hypervolemic Hyponatremia
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THE BALANCE Study: Treatment of Hyponatremia Based on Lixivaptan in NYHA Class III/IV Cardiac Patient Evaluation
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Read our methodology - how this data is sourced, computed, and verified.
Related
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