Trial record 2 of 2 for: "Bunion" | "Anesthetics, General"
A Safety Study of AQUAVAN® (Fospropofol Disodium) Injection for Sedation During Minor Surgical Procedures.
|ClinicalTrials.gov Identifier: NCT00327392|
Recruitment Status : Completed
First Posted : May 18, 2006
Results First Posted : June 20, 2012
Last Update Posted : June 20, 2012
Information provided by:
|Study Design||Allocation: Non-Randomized; Intervention Model: Single Group Assignment; Masking: None (Open Label); Primary Purpose: Diagnostic|
Drug: AQUAVAN® (fospropofol disodium) Injection
|Recruitment Details||This study recruited at 12 study centers in the US during the period of 22-Jun-2006 to 01 Mar 2007.|
|Pre-assignment Details||All subjects received fentanyl at an initial dose of 50 μg as an analgesic pretreatment 5 minutes prior to the administration of the initial dose of fospropofol disodium (also referred to as LUSEDRA and formerly known as AQUAVAN). After fentanyl administration, the venous catheter was flushed with 2 mL of sterile saline solution.|