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Clinical Trial Summary

The purpose of this study is to determine whether deep neuromuscular blockade compared to moderate neuromuscular blockade may improve the surgical conditions in patients undergoing laparoscopic bariatric surgery.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT02118844
Study type Interventional
Source Central Hospital, Nancy, France
Contact Thomas Fuchs-Buder, MD
Phone #33.383.153942
Email t.fuchs-buder@chu-nancy.fr
Status Recruiting
Phase Phase 4
Start date July 2014
Completion date April 2016

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