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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON31415

Enrollment

100

Registered

2007-06-28

Start date

2007-05-01

Completion date

Unknown

Last updated

2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

airway device breathingtube

Interventions

an Air-Q will be inserted in all patients. leakpressures are determined. when indicated, patients will be intubated through the Air-Q.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: patients undergoing general anesthesia in the ambulatory surgical unit of the ErasmusMC

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
first attempt succes rate	—

Secondary

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

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)