A Dose-ranging Study to Evaluate the Safety and Efficacy of LUSEDRA (Fospropofol Disodium) as an Intravenous Sedative for Diagnostic or Therapeutic Colonoscopy in Adult Special Populations
Clinical trial NCT01127438 · COMPLETED
Trial details
- NCT number
- NCT01127438
- Sponsor
- Eisai Inc.
- Status
- COMPLETED
- Phase
- Phase 4
- Study type
- INTERVENTIONAL
- Start date
- 2010-04-01
- Primary completion
- 2011-06-01
- Enrollment
- 153
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