Study about "emergence agitation" in patients underwent nasal surgery following general anesthesia according to anesthetic techniques

Comparison of the incidence and the severity of emergence agitation following general anesthesia during nasal surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002145

Enrollment

120

Registered

2016-11-18

Start date

2016-08-23

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others(anesthetic method) : Following randomised grouping into two groups (group TIVA:total intravenous anesthesia, group VA:volatile anesthesia), target-controlled infusion with propofol and remifent

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) patients planned nasal surgery under general anesthesia 2) over 17 year old 3) patents who approve to participate the study voluntaruly 4) patents in American Society of Anesthesia physical status 1-3

Exclusion criteria

Exclusion criteria: 1) patients who don't approve to participation 2) patients who have psychologic disease based on DSM-IV (Diagnostic and Statistical Manual of Mental Disorders-4th edition) 3) patients who have taken drugs including neuroleptics, benzodiazepine over 2 weeks within 1 month 4) history of allergy to opioids or NSAIDs(non-steroidal anti-inflammatory drugs) 5) diagnosed with asthma or nasal polyp 6) anyone who is not appropriate according to resercher's decision

Design outcomes

Primary

Measure	Time frame
intensity of sedation and agitation	—

Secondary

Measure	Time frame
intensity of postoperative pain	—

Countries

Korea, Republic of

Contacts

Public ContactJun-Young Jo

Asan Medical Center

junyoung.jo@gmail.com+82-2-3010-3868

Outcome results