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Comparison of two devices for intubation in COVID simulated scenario in mannequin

Comparison of King vision Videolaryngoscope channelled blade and Tuoren Videolaryngoscope non-channelled blade in a simulated COVID intubation scenario by novices and experienced anaesthesiologists: a prospective randomized crossover mannequin study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/06/025522
Enrollment
50
Registered
2020-06-01
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

None listed

Interventions

Intervention1: Intubation using Touren non channeled videolaryngosocpe with a styletted tube: The intubation will be done by anesthesiologist and non anesthesiologist in a mannequin in PPE using Toure

Sponsors

Research Section AIIMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Any anesthesiologist with atleast year experience in anesthesia and has performed more than 10 intubations with a VL earlier will be included. Any other medical personnel belonging to any other clinical domain (medicine, emergency medicine, cardiology, neurology, endocrinology etc) and being deployed to take care of suspected/ confirmed COVID19 patients.

Exclusion criteria

Exclusion criteria: Those who donot consent

Design outcomes

Primary

MeasureTime frame
Time to intubationTimepoint: Time to intubation

Secondary

MeasureTime frame
POGO score, CL grade, time to glottic view, number of intubation attempts, first attempt success rate, the number of optimization maneuvers required (re-adjustment of head position, second assistant) to aid tracheal intubation and the severity of dental trauma and ease of intubationTimepoint: All the parameters will be recorded during intubation in the mannequin

Countries

India

Contacts

Public ContactAnju Gupta

AIIMS

dranjugupta2009@rediffmail.com9911573371

Outcome results

None listed

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