Actively Recruiting
Can the STOP-Bang Questionnaire Predict Obstructive Sleep Apnea and Difficult Mask/Intubation in Patients Scheduled for Thoracic Surgery? Prospective Observational Study
Led by Atatürk Chest Diseases and Chest Surgery Training and Research Hospital · Updated on 2025-01-30
125
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Difficult airway management is a leading cause of problems during anesthesia, especially in patients with obstructive sleep apnea syndrome (OSAS). This study evaluates how well the STOP-BANG questionnaire can screen for OSAS and predict difficult mask ventilation and intubation in patients scheduled for thoracic surgery. The research aims to improve preparation for anesthesia by identifying patients at higher risk during surgery. Participants undergo assessment using the STOP-BANG questionnaire, which includes eight yes-or-no questions based on common risk factors for OSAS. Scores help categorize patients into low, moderate, or high risk for sleep apnea. The study observes airway management during surgery, classifying cases as easy airway or difficult airway based on mask ventilation assistance, oxygen levels, and intubation attempts. During the study, researchers monitor how the STOP-BANG score relates to actual airway difficulties encountered in surgery. Patients undergo evaluations including airway management observations and oxygen saturation monitoring during mask ventilation. The primary outcome is the STOP-BANG questionnaire result measured once within one month. Participation lasts through the surgery event and related assessments, with data collected to understand the relationship between questionnaire scores and airway challenges.
CONDITIONS
Brief Title
STOP-Bang Questionnaire: A Predictor of Obstructive Sleep Apnea and Difficult Mask/Intubation?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient undergoing thoracic surgery
- Age between 18 and 65 years
- ASA physical status classification 1 to 3
You will not qualify if you...
- History of obstructive sleep apnea syndrome
- History of previous head and neck surgery or radiotherapy
- Did not agree to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 month
Participants complete the STOP-Bang Questionnaire to assess the risk of obstructive sleep apnea prior to thoracic surgery.
1 time
Trial Site Locations
Total: 1 location
1
Ankara Atatürk Sanatorium Training and Research Hospital
Ankara, Keçiören, Turkey (Türkiye), 06290
Actively Recruiting
Research Team
A
Ali ALAGÖZ, professor
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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