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A Clinical trial to compare the airway protection of three airway devices air-Q, i-gel, LMA supreme in adult patients undergoing elective surgeries

Randomised comparison of the oropharyngeal leak pressure of air-Q with i-gel and larnyngeal mask airway supreme in anaesthetised adult patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/03/005623
Enrollment
75
Registered
2015-03-12
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- patients age between 18 years to 60 years of either sex belonging to ASA 1 and 2 who will be posted for elective surgeries.

Interventions

Intervention1: COMPARISON OF THREE AIRWAY DEVICES VIZ., air-Q, i-gel, LMA Supreme.: To compare the oropharyngeal leak pressure of all three above devices. Control Intervention1: TO COMPARE THREE AIRWA

Sponsors

Postgraduate institute of medical education and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2 patients elective surgeries in supine position

Exclusion criteria

Exclusion criteria: 1. Gastro-esophageal reflux disease 2. Prior Esophagectomy 3. Hiatus hernia 4. Prior h/o vomiting within 24hrs after surgery 5 .Known oropharyngeal morbidities 6. Full stomach with risk of aspiration 7. BMI >35kg/m2 8. Any condition which requires endotracheal intubation 9. Patients unwilling to participate in study.

Design outcomes

Primary

MeasureTime frame
OROPHARYNGEAL LEAK PRESSURETimepoint: 2 MINUTES AND 5 MINUTES AFTER INSERTION OF AIRWAY DEVICES

Secondary

MeasureTime frame
EASE OF GASTRIC TUBE PLACEMENTTimepoint: Maximum 3 times;EASE OF INSERTION OF DEVICETimepoint: able to ventilate effectively;EFFECTIVE AIRWAY INSERTION TIMETimepoint: Picking the device to appearance of Etco2;HEMODYNAMIC CHANGESTimepoint: 0,5,10,15,20,25,30,35 and 40 mins;NO OF ATTEMPTS TO INSERTTimepoint: Maximum 3 times;POST OPERATIVE COMPLICATIONSTimepoint: 0,6,12 and 24 hours

Countries

India

Contacts

Public ContactSRINATH D

PGIMER, CHANDIGARH

sameersethi29@gmail.com9317851002

Outcome results

None listed

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