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A Randomized, Controlled, Parallel-Group, Investigator-Initiated Trial toEvaluate the Efficacy, and Safety of the Use of Laryngeal Mask Compared toEndotracheal Intubation During Anesthesia in Pediatric Strabismus Surgery toPrevent Clinically Relevant Postoperative Nausea and Vomiting and Emergence Delirium UsingRisk-Adapted Postoperative Nausea and Vomiting Prophylaxis

Not Applicable
Conditions
R11
T88.5
F05.8
Nausea and vomiting
Other complications of anaesthesia
Other delirium
Registration Number
DRKS00029612
Lead Sponsor
niversitätsklinikum des Saarlandes, Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Enrolling by invitation
Sex
All
Target Recruitment
162
Inclusion Criteria

Subjects undergoing elective strabismus surgery under general anesthesia

Exclusion Criteria

Subjects with American Society of Anesthesiologists Physical Status Classification III or higher,
Subjects participating in another clinical trial

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of nausea and vomiting 6 hours postoperative
Secondary Outcome Measures
NameTimeMethod
Incidence of nausea and vomiting 2 and 24 hours postoperative,<br>Incidence of emergence delir,<br>other adverse events until discharge
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