- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05640856
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
Conditions
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-22/16
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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