A Comparison of LMA-Supreme and I-gel for the Incidence of Postoperative Sore Throat
- Conditions
- General Anesthesia
- Registration Number
- NCT02745964
- Lead Sponsor
- Yonsei University
- Brief Summary
The purpose of this study is to investigate and compare the incidence of the postoperative sore throat between LMA supreme and I-gel.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 8
- adult patients aged over 19 years who are scheduled for elective surgery under general anesthesia using the laryngeal mask airway
- Anticipated difficult airway
- Expected duration of surgery more than 4 hours
- body mass index more than 35 kg/m2
- pregnancy
- Upper gastrointestinal surgery or open abdominal surgery.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Postoperative sore throat within 24 hours after the end of surgery. The postoperative sore throat will be evaluated after the end of surgery by the investigator who are blinded to the group assignments. The investigator will ask the participant about his/her sore throat status.
- Secondary Outcome Measures
Name Time Method Postoperative dysphagia within 24 hours after the end of surgery The postoperative dysphagia will be evaluated after the end of surgery by the investigator who are blinded to the group assignments. The investigator will ask the participant about his/her status.
Postoperative dysphonia within 24 hours after the end of surgery The postoperative dysphonia will be evaluated after the end of surgery by the investigator who are blinded to the group assignments. The investigator will ask the participant about his/her status.
Trial Locations
- Locations (1)
Department of Anesthesiology and Pain MedicineSeverance Hospital, Yonsei University Health System
🇰🇷Seoul, Korea, Korea, Republic of
Department of Anesthesiology and Pain MedicineSeverance Hospital, Yonsei University Health System🇰🇷Seoul, Korea, Korea, Republic of