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Evaluation of successful intubation under general anaesthesia through a device called i-gel Plus in patients who will undergo anaesthesia and has no contraindication for the device insertion.

Evaluation of first pass success rate of intubation through i-gel Plus in anesthetized patients without anticipated difficult airway - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100405
Enrollment
62
Registered
2026-01-06
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: R198- Other specified symptoms and signsinvolving the digestive system and abdomen

Interventions

Intervention1: Intubation through igel Plus in anesthetized patients without anticipated difficult airway: To assess the safety and feasibility of endotracheal intubation using the i-gel Plus as a co

Sponsors

Kasturba Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age between 18 to 60 years Patients with American Society of Anesthesiologists physical status I and II requiring general anesthesia with endotracheal intubation

Exclusion criteria

Exclusion criteria: Patient refusal Patients with predictors of difficult bag and mask ventilation Patients with predictors of difficult supraglottic airway device placement Patients with predictors of difficult laryngoscopy Patients with an anticipated difficult airway with a Wilson score more than 5 as assessed in preoperative airway examination Patients with increased risk of aspiration, such as morbid obesity and pregnancy Patients with body mass index BMI more than 30 Patients with obstructive airway pathology and reactive airway disease Patients undergoing airway surgeries

Design outcomes

Primary

MeasureTime frame
To evaluate the first pass success rate of intubation through i-gel Plus Timepoint: 0min 1min

Secondary

MeasureTime frame
Fibreoptic grade of visualization of the glottis, ease, time, attempts & success of device placement, time for successful endotracheal intubation, & complications if notedTimepoint: 0min 1min

Countries

India

Contacts

Public ContactShweta Sinha

Manipal Academy of Higher Education

shweta.sinha@manipal.edu9113041764

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026