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trial of breathing tube through two airway devices

Comparison of Intubating laryngeal mask airway and I gel airway as a conduit for blind endotracheal intubation

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/06/006997
Enrollment
120
Registered
2016-06-06
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 of either sex, in the age group 18 â?? 60 years belonging to ASA physical status I-II, weighing 50 â?? 90 kg and scheduled for elective surgical procedures requiring tracheal intubation

Interventions

Intervention1: I- gel airway: Flexible silicone tube (FST) used to intubate through I-gel airway Control Intervention1: Inubating laryngeal mask airway : Flexible silicone tube (FST) used to intubate

Sponsors

Post Graduate Institute of Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I-II,weighing 50 â?? 90 kg and scheduled for elective surgical procedures requiring tracheal intubation were included in the study.

Exclusion criteria

Exclusion criteria: ASA III-V patients, contraindication to use of muscle relaxants, anticipated or known difficult intubation or ventilation and patients at increased risk of aspiration or having a history of symptomatic gastroesophageal reflux or hiatal hernia.

Design outcomes

Primary

MeasureTime frame
Rate of successful intubation in first attemptTimepoint: number of successful intubation in first attempt. After intubation through the airway device whether ETCO2 graph appears or not was noted in first attempt( If ETCO2 graph detected on the monitor, intubation was considered successful)

Secondary

MeasureTime frame
overall success rate, ease of SGA insertion and intubation, time to SGA insertion and intubation and adverse events.Timepoint: Time taken to insert the airway was noted from holding the device to successfully inserting the device. Time taken to intubation was noted from holding the tube in hand to successful intubation. i e appearance of ETCO2 curve on the monitor. Adverse events like sore throat, horseness, vocal cord paralysis was assessed soon after extubation and 24 hours after the procedure

Countries

India

Contacts

Public ContactDr Neerja Bhardwaj

PGIMER

neerja.bhardwaj@gmail.com01722756500

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 2, 2026