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Comparison of two supraglottic airway devices air-Q ILA and i â??gel for maintaining ventilation under general anaesthesia

Comparison of air-Q ILA and i â??gel supraglottic device in airway management during general anaesthesia â?? a randomised controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/06/005905
Enrollment
70
Registered
2015-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- â?? ASA class 1 & 2 patients requiring general anaesthesia for elective surgery in JIPMER of age 18 to 60 year

Interventions

Intervention1: air q: air-Q® Masked Laryngeal Airways Disposable(mercury medicals) will be secured under standard anaesthesia technique. Intubation through the airway channel of air-Q® will be atte

Sponsors

JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA class 1 & 2 patients requiring general anaesthesia for elective surgery in JIPMER

Exclusion criteria

Exclusion criteria: 1 Any pathology of the neck, upper respiratory tract or upper alimentary tract. 2 Predicted difficult airway, 3 A body mass index >35 kg/m2. 4 Patients with history of obstructive sleep apnea. 5 Patients at risk of pulmonary aspiration of gastric contents

Design outcomes

Primary

MeasureTime frame
To compare the success rate of endotracheal intubation through both devicesTimepoint: during perioperative period

Secondary

MeasureTime frame
To compare the following parameters in both devices No of attempts in device insertion and endotracheal intubation Ease of insertion of S.G.A Device insertion time and ET intubation time Device removal time Timepoint: during perioperative period

Countries

India

Contacts

Public ContactBALAJI K

JIPMER

sumanlatagupta13@gmal.com9488830091

Outcome results

None listed

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