Optimal Stylet for video-laryngoscope Intubation Using the hyperangulated blade; randomized controlled study
Not Applicable
- Conditions
- Injury, poisoning and certain other consequences of external causes
- Registration Number
- KCT0008951
- Lead Sponsor
- Samsung Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 180
Inclusion Criteria
-Patients requiring endotracheal intubation under general anesthesia
-American Society of Anesthesiologists (ASA) class I - III
-Individuals who have consented to participate in a clinical trial and have signed the informed consent form
Exclusion Criteria
Individuals deemed unsuitable for participation in a clinical trial based on the investigator's judgment (e.g., risk of dental damage, anticipation of a highly difficult intubation such as Mallampati grade 4, head and neck mass)
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method duration of the entry of the video laryngoscope into the mouth until the complete removal of the stylet
- Secondary Outcome Measures
Name Time Method