The Air-Q laryngeal mask airway during anesthesia with controlled ventilation: a clinical trial of efficacy

• Conditions: airway device; breathingtube; 10043413

• Registration Number: NL-OMON31415
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

patients undergoing general anesthesia in the ambulatory surgical unit of the ErasmusMC

Exclusion Criteria

known or expected difficult intubation
preexistant obstructive airway problems
BMI >30
patients in need of rapid sequence induction

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>first attempt succes rate</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- time to first breath<br /><br>- Leakpressure<br /><br>- first attempt succesrate endotracheal intubation<br /><br>- cuffpressure<br /><br>- hemodynamic reaction to insertion<br /><br>- end-tidal CO2 and periferal oxygensaturation<br /><br>- any episodes of coughing, hiccup, laryngospasm and brochospasm<br /><br>- presence of blood on the cuff of the Air-Q at extubation<br /><br>- sore throat, dysphonia and dysphagia after extubation</p><br>