Protocol for Eslax Intravenous Drug Use Investigation (Study P06082)

Status Completed

Clinical Trial Summary

The main purpose of this investigation is to collect safety and efficacy information of Eslax Intravenous 25mg/2.5mL and 50mg/5.0mL (hereinafter referred to as "Eslax") in daily clinical settings.

Clinical Trial Description

Post-marketing surveys are not considered applicable clinical trials and thus the results of this survey will not be posted at its conclusion. The results will be submitted to public health officials as required by applicable national and international laws. ;

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Anesthesia

Clinical Trial Details

NCT number	NCT00902070
Study type	Observational
Source	Merck Sharp & Dohme Corp.
Contact
Status	Completed
Phase	N/A
Start date	November 2007
Completion date	October 2010

View Details

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