A PK/PD Study of Fospropofol Disodium Compared With Propofol Injectable Emulsion

Completed · Phase 4

Conditions studied: Anesthesia

In brief

This study is designed to characterize the pharmacokinetic and pharmacodynamic effect of fospropofol disodium in comparison to propofol. In addition, the study will compare the maximum sedative effect, safety and tolerability of fospropofol disodium and propofol.

Key facts

Study ID

NCT01260142

Run by

Eisai Inc.

People needed

36

Starts

2010-11-01

Expected to finish

2011-03-01

Last updated by the study team

2017-01-27

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

Where it is running

• Duke University Medical Center — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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