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Comparison of three airway devices for general anaesthesia

A Randomised Comparative Study of Three Supraglottic Airway Devices for Controlled Ventilation in Anaesthetised Paralysed Patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023588
Enrollment
270
Registered
2020-02-26
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- surgical patients

Interventions

Intervention1: LMA ProSeal: The ProSeal laryngeal mask airwayâ?¢ (PLMA) is an extensively used device and is a prototype of 2nd generation LMAs. It is a directional perilaryngeal sealer. It has a uniq

Sponsors

Sir Ganga Ram Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age 18 years or more 2) ASA physical status 1 to3 3) Fasting more than 6 hours

Exclusion criteria

Exclusion criteria: 1) patients who have not fasted 2) patients with anticipated difficult airway 3) patients with inadequate mouth opening to permit insertion of device 4) patients for emergency surgery 5) Patients who are prone to aspiration 6) patients with BMI more than 40 kg/m2 7) patients requiring tracheal intubation.

Design outcomes

Primary

MeasureTime frame
Oropharyngeal seal pressure (OSP)Timepoint: From induction to 5 minutes after induction

Secondary

MeasureTime frame
1) Fiberoptic confirmation of anatomical position 2) Ease of insertion 3) First attempt insertion success rate (%) 4) Number of attempts for insertion of gastric tube 5) Pharyngolaryngeal morbidity Sore throat/dysphonia/dysphagia 6) Other adverse eventsTimepoint: From induction to 2hrs post operatively

Countries

India

Contacts

Public ContactDr Manoj Sharma

SIR GANGA RAM HOSPITAL, NEW DELHI

bimsharma@rediffmail.com9810135366

Outcome results

None listed

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