Clinical Trials Directory

Trials / Unknown

UnknownNCT03398759

Butorphanol Mitigate Emergence Agitation in Patients Undergoing Functional Endoscopic Sinus Surgery

Butorphanol Mitigate Emergence Agitation in Patients Undergoing Functional Endoscopic Sinus Surgery:a Randomized Control Double Blinded Clinical Trail

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
700 (estimated)
Sponsor
RenJi Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGButorphanolIV injection during induction
DRUGPlacebosIV injection during induction

Timeline

Start date
2018-02-01
Primary completion
2020-12-31
Completion
2020-12-31
First posted
2018-01-12
Last updated
2020-03-10

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03398759. Inclusion in this directory is not an endorsement.