Clinical evaluation of the Portex single use laryngeal mask airway in paediatric anaesthesia: a randomised controlled study with the Intavent "classic" laryngeal mask airway

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN07684370

Enrollment

Registered

2004-09-30

Start date

2003-09-26

Completion date

Unknown

Last updated

2015-01-13

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

Conditions

Surgery: Anaesthesia Surgery Anaesthesia

Interventions

1. Single use Portex laryngeal mask 2. Intavent 'classic' laryngeal mask

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing elective surgery

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

Measure	Time frame
Securing a safe airway	—

Secondary

Measure	Time frame
Number of insertion attempts, time to satisfactory insertion, ease of insertion, presence of a post op sore throat	—

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026