Skip to content

A Comparative study between two methods of ventilating bougie guided tracheal intubation through I-gel.

A Randomized Controlled Study to compare the Blind approach versus the Ultrasound guided tracheal intubation over ventilating bougie through I-gel.

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018142
Enrollment
360
Registered
2019-03-18
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: 8- Other Procedures

Interventions

Intervention1: Ultrasound guided: Ultrasound guided ventilating bougie insertion through I-gel followed by ultrasound guided endotracheal intubation over the ventilating bougie after removal of I-gel.

Sponsors

Dr Anisha Pauline P
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists Physical Status Grade I or II, Body weight between 40 - 70 kg, Normal Airway (Mallampati Grade I or II, Posted for elective surgery requiring general anaesthesia and endotracheal intubation.

Exclusion criteria

Exclusion criteria: American Society of Anaesthesiologists Physical Status Grade III and above, Obesity (BMI greater than 25), Mallampati Grade III or IV, History of gastro-oesophageal reflux disease, inadequate fasting, any known or anticipated difficult tracheal intubation or face mask ventilation

Design outcomes

Primary

MeasureTime frame
To compare the first attempt success of endotracheal intubation over ventilating bougie through I-gel either through blind approach or by busing ultrasound guided method.Timepoint: Till 5 minutes after endotracheal intubation

Secondary

MeasureTime frame
Number of attempts and time for insertion of I-gel, number of attempts and time for insertion for ventilating bougie, total intubation time, hemodynamics upto 5 minutes after endotracheal intubation and adverse events.Timepoint: Immediate post op period upto 2 hours

Countries

India

Contacts

Public ContactDr Anisha Pauline P

Sri Ramachandra University

dr.anishapauline@gmail.com9994247287

Outcome results

None listed

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