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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06441175
Other study ID # CP during videolaryngoscopy
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 1, 2024
Est. completion date July 1, 2026

Study information

Verified date May 2024
Source Seoul National University Hospital
Contact TAE KYONG KIM
Phone 82-2-870-2519
Email ktkktk@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare the success rate of upper esophageal obstruction with cricoid pressure during videolaryngoscopy and direct laryngoscopy.


Description:

Even with appropriate cricoid pressure, the lifting force of the laryngoscope during direct laryngoscopy for tracheal intubation may counteract the cricoid pressure, making esophageal obstruction ineffective. Compared to direct laryngoscopy, videolaryngoscopy requires less lifting force, and thus, the success rate of esophageal obstruction may be higher. This study aims to compare the success rate of upper esophageal obstruction with cricoid pressure during videolaryngoscopy and direct laryngoscopy.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 140
Est. completion date July 1, 2026
Est. primary completion date July 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients scheduled to have general anesthesia with tracheal intubation Exclusion Criteria: - Gastroesophageal reflux disease, achalasia, bowel obstruction, - BMI > 35 kg/m2 - Uncontrolled diabetes - Pregnancy - Previous esophageal, and gastric surgery - Dental damage or anticipated difficult airways - Who do not consent to the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intubation device order
D-V group: the group that performs direct laryngoscopy first and then videolaryngoscopy. V-D group: the group that performs video laryngoscopy first and then directlaryngoscopy."

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Seoul National University Hospital SMG-SNU Boramae Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary Success rate of esophageal obstruction during cricoid pressure Success rate of esophageal obstruction during cricoid pressure During general anesthesia induction
Secondary Esophageal diameter Esophageal diameter measured by ultrasound During cricoid pressure
Secondary percentage of glottic opening score percentage of glottic opening During cricoid pressure
Secondary Cormack-Lehane grade views obtained by laryngoscopy During cricoid pressure
See also
  Status Clinical Trial Phase
Completed NCT03908411 - The Effect of Paratracheal Pressure on the Glottic View N/A
Completed NCT02161601 - Effect of Incorrectly Applied Cricoid Pressure During Rapid Sequence Induction. Evaluation With High-resolution Manometry. N/A
Completed NCT04135651 - Paratracheal Esophagus Pressure on the Intubation With Pentax Airway Scope N/A