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Dexmedetomidine for Postoperative Analgesia After Bariatric Surgery

Obesity Clinical Trial

Official title:
Intraoperative Dexmedetomidine Versus Morphine for Postoperative Analgesia After Laparoscopic Bariatric Surgery

Clinical Trial Summary

The purpose of this study is to determine if Dexmedetomidine given at the end of surgery will reduce postoperative morphine consumption and improve postoperative quality of recovery as compared to morphine in patients undergoing laparoscopic bariatric surgery.

Clinical Trial Description

effect of Dexmedetomidine bolus on postoperative morphine requirements ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02213159
Study type Interventional
Source American University of Beirut Medical Center
Contact
Status Completed
Phase Phase 2/Phase 3
Start date July 2014
Completion date December 2015
View Details
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