Relationship Between STOP BANG Score and Airway Management

November 28, 2022 updated by: Bengü Gülhan Köksal, Zonguldak Bulent Ecevit University

Evaluation of Relationship Between Oxygen Reserve Index and Difficult Airway With Stop Bang Score

Nowadays, anesthetists may encounter many patients who are not diagnosed with obstructive sleep apnea syndrome (OSAS) to undergo elective surgery. Recognition of these patients by anesthesiologists and taking necessary precautions will significantly reduce perioperative complications and mortality. STOP-BANG is a questionnaire used to predict high risk of OSAS. The aim of our study is to evaluate the clinical use of the oxygen reserve index as an early warning of possible desaturation in patients with low and high risk of OSAS according to the Stop Bang score.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

1

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 Bülent Ecevit University Medicine Faculty

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients aged 18-65 to be intubated undergoing elective surgery

Description

Inclusion Criteria:

  • American Society of Anesthesiologists (ASA) I-III
  • Between 18-65 years old
  • Volunteered to participate in the study

Exclusion Criteria:

  • diagnosed with asthma, COPD, heart failure or coronary artery disease, OSAS
  • morbidly obese (BMI>45 kg/m2),
  • patients with a history of alcohol or drug addiction
  • women in pregnancy or lactation
  • allergic to the drugs used in the study

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Group D
STOP BANG Score <3
Endotracheal tube placement
Group Y
STOP BANG Score ≥ 3
Endotracheal tube placement

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of Oxygenation
Time Frame: up to intubation
prediction of desaturation by oxygen reserve index in patients with low and high risk of OSAS
up to intubation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of difficult Airway
Time Frame: up to intubation
using mask-ventilation scale in patients with low and high risk of OSAS
up to intubation

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)

January 1, 2021

Primary Completion (Actual)

June 30, 2022

Study Completion (Actual)

November 1, 2022

Study Registration Dates

First Submitted

November 16, 2022

First Submitted That Met QC Criteria

November 28, 2022

First Posted (Estimate)

December 7, 2022

Study Record Updates

Last Update Posted (Estimate)

December 7, 2022

Last Update Submitted That Met QC Criteria

November 28, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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