Viewing Study NCT00363935


Ignite Creation Date: 2025-12-24 @ 10:39 PM
Ignite Modification Date: 2025-12-31 @ 1:28 PM
Study NCT ID: NCT00363935
Status: WITHDRAWN
Last Update Posted: 2019-01-16
First Post: 2006-08-10
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Bariatric Dose-ranging Study With Dexmedetomidine
Sponsor: University of Texas Southwestern Medical Center
Organization:

Study Overview

Official Title: A Randomized, Double-blind, Controlled Study of Dexmedetomidine (Precedex) Infusion for Improving Control of Acute Autonomic Response During Laparoscopic Bariatric Surgery
Status: WITHDRAWN
Status Verified Date: 2019-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: After obtaining informed consent,80 morbidly obese ASA II-III patients undergoing laparoscopic bariatric surgery procedures would be randomly assigned to one of four study groups at UTSWMC at Dallas.Hemodynamic paarameters, recovery times, postoperative pain scores, the need for rescue analgesics and side effects will be recorded.The purpose of this study is to determine the optimal linfusion rate of dexmedetomidine for maintaining cardiovscular stability during general anesthesia.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: