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
| Type | Name | Description |
|---|---|---|
| DRUG | Butorphanol | IV injection during induction |
| DRUG | Placebos | IV 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.