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Clinical Trial Summary

Emergence agitation is one of the common postoperative complications after functional endoscopic sinus surgery(FESS). The objective of present study is to explore the effectiveness of butorphanol in the alleviation of emergence agitation in patients undergoing Functional Endoscopic Sinus Surgery.


Clinical Trial Description

Butorphanol is a mixed agonist-antagonist opioid with strong κappa-receptor agonist and weak mu-receptor antagonist activity. It is commonly used for the management of cancer, postoperative, gynecologic, and obstetric pain. Additionally, Butorphanol has less respiratory depression and sedation effects, which make it may become a good medicine to alleviate the agitation. However, there is no clinical evidence to confirmation of such effectiveness of butorphanol. The objective of present study is to explore the effectiveness of butorphanol in the alleviation of emergence agitation in patients undergoing Functional Endoscopic Sinus Surgery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03398759
Study type Interventional
Source RenJi Hospital
Contact Xiaorong Huai, MS
Phone +8613818003683
Email smile_huai@126.com
Status Recruiting
Phase N/A
Start date February 1, 2018
Completion date December 31, 2020

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