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Study to Determine if Administration of Sugammadex Impacts Hospital Efficiency

Neuromuscular Blockade Clinical Trial

Official title:
A Randomized, Blinded-assessor, Single Center Study to Determine if Administration of Sugammadex, When Used to Reverse Deep Neuromuscular Blockade (NMB) After Open Abdominal Surgery, Impacts Hospital Efficiency

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy of Sugammadex in rapidly reversing deep neuromuscular blockaded (induced by rocuronium)

Clinical Trial Description

Participants in the study group will receive a single bolus of Sugammadex (4.0mg/kg) prior to extubation. In the post-anesthesia care unit (PACU), a blinded safety-assessor will use the visual analog scale to clinically assess post-operative pain. Post-operative nausea and vomiting (PONV) will be assessed using a PONV rating scale every 30 minutes until PACU discharge. All patients will be monitored with continuous pulse-oximetry. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02860507
Study type Interventional
Source University of South Florida
Contact
Status Completed
Phase Phase 4
Start date August 2016
Completion date February 2018
View Details
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