Desflurane in Children With Laryngeal Mask Airway
Not Applicable
Completed
- Conditions
- Desflurane Anesthesia
- Interventions
- Drug: Sevoflurane/Desflurane
- Registration Number
- NCT02470442
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
The purpose of this study is to characterize the airway responses to desflurane during maintenance of and emergence from anesthesia in children whose airways were supported with laryngeal mask airways (LMAs).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
- scheduled for elective surgery under general anesthesia with laryngeal mask airway
Exclusion Criteria
- history of reactive airways disease with an acute exacerbation within the past 2 weeks
- if wheezing or an active upper respiratory infection was present on the day of surgery
- if there was a history of malignant hyperthermia
- a history of moderate-to-severe hepatic dysfunction following anesthesia with desflurane not otherwise explained.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Sevoflurane/Desflurane Sevoflurane/Desflurane After induction of general anesthesia with sevoflurane, anesthesia was maintained with desflurane. Sevoflurane Sevoflurane the anesthetic induction and maintenance with sevoflurane.
- Primary Outcome Measures
Name Time Method respiratory adverse events participants will be followed for postoperative period, an expected average of 30 minutes.
- Secondary Outcome Measures
Name Time Method emergence agitation 15 minutes after arrival on PACU
Trial Locations
- Locations (1)
Seoul national university hospital
🇰🇷Seoul, Korea, Republic of