Clinical trial
Study of AQUAVAN® Injection (AQUAVAN; Fospropofol Disodium) for Sedation During…
NCT00125424 · Eisai Inc., Industry · Completed
Key facts
| NCT number | NCT00125424 |
|---|---|
| Title | Study of AQUAVAN® Injection (AQUAVAN; Fospropofol Disodium) for Sedation During Colonoscopy |
| Official title | A Randomized, Double-Blind, Dose-Response Study to Assess the Efficacy and Safety of AQUAVAN® Injection for Procedural Sedation in Patients Undergoing Colonoscopy |
| Lead sponsor | Eisai Inc., Industry |
| Status | Completed |
| Phase | Phase 2/Phase 3 |
| Study type | Interventional |
| Conditions | Colonoscopy, Colonic Polyps |
| Intervention type | Drug |
| Interventions | AQUAVAN® (fospropofol disodium) Injection, Midazolam HCl |
| Enrollment | 125 |
| Start date | Jul 1, 2005 |
| Completion | Sep 1, 2005 |
| First posted | Aug 1, 2005 |
| Last update posted | Nov 7, 2008 |
| Countries | United States |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: