Race-Specific Propofol Titration to Effect for Procedural Sedation

Status Completed

Clinical Trial Summary

Prospectively evaluate newly established guidelines and make clinicians aware of inter-racial difference in propofol sensitivity.

Clinical Trial Description

The primary motivation in conducting this study is to conduct the implementation science, i.e., formalize and train, and retrain if needed, anesthesia providers in the standard practice of titrating infusion rate to effect and clinically evaluate the effect of race and ethnicity on propofol monotherapy sedation during GI endoscopy. The ultimate goal is to make it less likely that patients from races known to be sensitive to propofol experience inadvertent overdosing. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03290859
Study type	Observational
Source	University of Florida
Contact
Status	Completed
Phase
Start date	January 5, 2018
Completion date	February 5, 2019

View Details

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