Glottic Opening Percentage (POGO) With Miller and McGrath MAC Videoingoscopes

April 14, 2023 updated by: Gamze Küçükosman, Zonguldak Bulent Ecevit University

Comparison of Glottic Opening Percentage (POGO) With Miller and McGrath MAC Videoingoscopes According to Direct Epiglottis Lifting Method

The aim of this study is to compare the percentage of glottic opening (POGO) with Miller and McGrath MAC Videoingoscopes compared to the direct epiglottis lifting method.

Study Overview

Detailed Description

The aim of this study is to compare the percentage of glottic opening (POGO) with Miller and McGrath MAC Videoingoscopes compared to the direct epiglottis lifting method.

Study Type

Observational

Enrollment (Actual)

85

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kozlu
      • Zonguldak, Kozlu, Turkey, 67600
        • Zonguldak Bulent Ecevit University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Probability Sample

Study Population

85 patients 18-65 years both genders in all surgeries requiring intubation

Description

Inclusion Criteria:

  • Those who agreed to participate in the study
  • He will undergo elective surgery
  • Endotracheal intubation required
  • 18-65 years old
  • ASA 1-2 risk
  • Body mass index<30
  • No risk of difficult intubation

Exclusion Criteria:

  • Those who do not want to participate in the study,
  • Allergic to study drugs,
  • Pregnant women
  • Those with a history of difficult intubation
  • They will be applied rapid-serial intubation
  • Emergency

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Group M (n=42), Miller laryngoscope
The effect of direct epiglottis lifting method on the percentage of glottic patency in Miller and McGraht laryngoscopy.
The percentage of glottic opening (POGO) will be evaluated according to the method of lifting the epiglottis (direct imaging).
Group V (n= 43), McGrath MAC videolaryngoscope
The effect of direct epiglottis lifting method on the percentage of glottic patency in Miller and McGraht laryngoscopy.
The percentage of glottic opening (POGO) will be evaluated according to the method of lifting the epiglottis (direct imaging).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of Glottic Opening Percentage (POGO) With Miller and McGrath MAC Videolaryngoscopes According to Direct Epiglottis Lifting Method
Time Frame: during laryngoscopy
Comparison of Glottic Opening Percentage (POGO) With Miller and McGrath MAC Videolaryngoscopes According to Direct Epiglottis Lifting Method
during laryngoscopy

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2022

Primary Completion (Actual)

December 31, 2022

Study Completion (Actual)

December 31, 2022

Study Registration Dates

First Submitted

March 24, 2023

First Submitted That Met QC Criteria

April 14, 2023

First Posted (Actual)

April 19, 2023

Study Record Updates

Last Update Posted (Actual)

April 19, 2023

Last Update Submitted That Met QC Criteria

April 14, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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