drugset / Trial / NCT00690495

Use of a Modified Propofol Emulsion in Adults

NCT00690495

Phase 3 Completed 100 enrolled B. Braun Melsungen AG
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of the study is to determine whether a modified propofol preparation shows any effect on the incidence of injection pain in adults undergoing elective surgery under general anesthesia. Study hypothesis: The use of a modified propofol preparation will reduce the incidence of injection pain in the study group.

Timeline

Start
2008-05
Primary completion
2008-09
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Propofol Small molecule 0.5 % Intravenous
Subject Propofol Small molecule 1 % Intravenous

Indications

No indication recorded.