Skip to content

Anesthesiology Trainees Performing Flexible Scope Intubation in Patients in the Left Lateral Position and the Supine Position: A Prospective Randomized Trial

Anesthesiology Trainees Performing Flexible Scope Intubation in Patients in the Left Lateral Position and the Supine Position: A Prospective Randomized Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200208001
Enrollment
40
Registered
2020-02-08
Start date
2020-02-10
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Difficult airway Difficult intubation Upper airway obstruction Intubating fibreoptic bronchoscope Flexible intubation scope Fiberoptic intubation Difficult airway Difficult intubation Upper airway obstruction Intubating fibreoptic bronchoscope Flexible intubation scope Fiberoptic intubation

Interventions

Flexible scope intubation in the left lateral position,Flexible scope intubation in the supine position
Experimental Device,Experimental Device

Sponsors

No sponsor
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Healthy patients who undergoing general anesthesia with endotracheal tube intubation

Exclusion criteria

Exclusion criteria: -Expected difficult airway -Low cardiopulmonary reserve patient -Unable to position in lateral position -Allergy to drug that will given for general anaesthesia -Reject flexible scope intubation

Design outcomes

Primary

MeasureTime frame
Success rate in intubation During the intervention Success rate in intubation less than 5 minute

Secondary

MeasureTime frame
Intubation time During the intervention Intubation time in second,Attempt(s) of intubation During the intervention Numbers of attempt(s),Change of vital signs at 1 minute after end of the intervention Vital signs before and after intubation 1 minute,Patient satisfactory at 24 hours after end of the intervention Report of patient (hoarseness, sore thoart)

Countries

Thailand

Contacts

Public ContactPoonyanuch Charoenkoop

Unaffiliated

s.poonyanuch@gmail.com66814941718

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026