drugset / Trial / NCT01271569

A Study to Assess the Efficacy and Safety of Fospropofol Disodium

NCT01271569

Phase 1 Completed 80 enrolled West China Hospital
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The aim of this study was to evaluate the pharmacodynamics, safety, and tolerability of Fospropofol disodium up to a dose producing maximal hypnotic effect as defined by electroencephalogramderived assessment (Bispectral Index \[BIS\]) and to compare the dynamic properties of PropofolF to those of Propofol.

Timeline

Start
2010-03
Primary completion
2010-09
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject fospropofol Small molecule 0.5 g

Indications

No indication recorded.