Clinical trial

An Effectiveness and Safety Study of AQUAVAN® Injection (Fospropofol Disodium)…

NCT00261599 · Eisai Inc., Industry · Completed

Key facts

NCT number NCT00261599
Title An Effectiveness and Safety Study of AQUAVAN® Injection (Fospropofol Disodium) for Sedation During Colonoscopy
Official title A Phase 3, Randomized, Double-Blind, Dose-Controlled Study to Assess the Efficacy and Safety of AQUAVAN® (Fospropofol Disodium) Injection for Minimal to Moderate Sedation in Patients Undergoing Colonoscopy
Lead sponsor Eisai Inc., Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Conscious Sedation
Intervention type Drug
Interventions AQUAVAN® (fospropofol disodium) Injection, Midazolam HCI
Enrollment 300
Start date Mar 1, 2006
Completion Oct 1, 2006
First posted Dec 5, 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:

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