Glottis Visualization in Different Lifting Methods

• Sponsor: Zonguldak Bulent Ecevit University (Other)
• Overall Status: Completed
• CT.gov ID: NCT05967338
• Collaborator: (none)
• Enrollment: 1
• Location: 1
• Actual Duration (Months): 8
• Patients Per Site Per Month: 0.1

Study Details

Study Description

Brief Summary

Among the various types of video laryngoscopes, the McGrath MAC video laryngoscopy (VL) has become popular because it is lightweight and can be quickly and hygienically prepared by changing the blade. The aim of this study was to compare the efficacy of two different methods (direct and indirect) for epiglottis removal during visualization of the glottis using the McGrath MAC VL.

Condition or Disease	Intervention/Treatment	Phase
Intubation; Glottis Visualization	Device: using McGrath Video Laryngoscope

Study Design

• Study Type: Observational
• Actual Enrollment: 1 participants
• Observational Model: Cohort
• Time Perspective: Prospective
• Official Title: Comparison of Epiglottis Lifting Methods Using a McGrath Video Laryngoscope: Direct vs. Indirect
• Actual Study Start Date: Jul 1, 2022
• Actual Primary Completion Date: Jan 30, 2023
• Actual Study Completion Date: Mar 1, 2023

Arms and Interventions

Arm	Intervention/Treatment
Group Direct glottis visualization in direct lifting	Device: using McGrath Video Laryngoscope; glottis visualization in indirect and direct lifting methods by using McGrath Video Laryngoscope
Group Indirect glottis visualization in indirect lifting	Device: using McGrath Video Laryngoscope; glottis visualization in indirect and direct lifting methods by using McGrath Video Laryngoscope

Outcome Measures

Primary Outcome Measures

1. POGO scores [1 day (through intubation )]

   percentage of glottic opening

Secondary Outcome Measures

1. Cormack-Lehane classification [1 day (through intubation )]

   assessment of laryngeal view during laryngoscopy

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 65 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• ASA I-II

• general anesthesia in elective surgeries

• 18-65 years old

• body mass index (25-30)

• no risk of difficult intubation

Exclusion Criteria:

• Allergic to study drugs

• pregnant women

• emergency cases

• those with a history of difficult intubation

• those without consent

• those at risk of aspiration

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Zonguldak Bülent Ecevit University	Zonguldak	Kozlu	Turkey	67600

Sponsors and Collaborators

• Zonguldak Bulent Ecevit University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Keziban Bollucuoglu, Principal Investigator, Zonguldak Bulent Ecevit University
• ClinicalTrials.gov Identifier: NCT05967338
• Other Study ID Numbers: 2022/12-10
• First Posted: Aug 1, 2023
• Last Update Posted: Aug 1, 2023
• Last Verified: Jul 1, 2023

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Keziban Bollucuoglu, Principal Investigator, Zonguldak Bulent Ecevit University: Endotrakeal intubation; Epiglottis; Glottis; McGrath MAC video laryngoscope

Study Results

No Results Posted as of Aug 1, 2023