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Clinical Trial Summary

The current study aims to elucidate the effectiveness of a preventative delirium protocol in patients older than 65 years of age undergoing elective surgery.


Clinical Trial Description

A comprehensive analysis of patient specific risk factors and predisposing perioperative risk factors will be completed. The objective is to see if delirium incidences are significantly lower in the group that receives a preventative delirium protocol compared to a control group, while not increasing other adverse undesirable side effects. We hypothesize that a preventative delirium protocol will reduce the incidence of delirium compared to the control group (primary outcome), but this protocol may lead to increased side effects such as PONV, poor pain control, and increased awareness (secondary outcomes). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03591120
Study type Interventional
Source Rush University Medical Center
Contact Robert J McCarthy, PharmD
Phone 312-942-7608
Email Robert_J_McCarthy@rush.edu
Status Recruiting
Phase N/A
Start date May 1, 2016
Completion date August 1, 2021

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