Using the STOP-BANG questionnaire to predict obstructive sleep apnea and difficult intubation in thoracic surgery patients
Can the STOP-Bang Questionnaire Predict Obstructive Sleep Apnea and Difficult Mask/Intubation in Patients Scheduled for Thoracic Surgery? Prospective Observational Study
This study is testing if the STOP-BANG questionnaire can help predict sleep apnea and difficult intubation in patients aged 18-65 who are having thoracic surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 125 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Atatürk Chest Diseases and Chest Surgery Training and Research Hospital Academic / other |
| Locations | 1 site (Ankara, Keçiören) |
| Trial ID | NCT06247631 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the effectiveness of the STOP-BANG questionnaire as a screening tool for obstructive sleep apnea syndrome (OSAS) in patients undergoing thoracic surgery. It investigates how well this questionnaire can predict the likelihood of difficult mask ventilation and intubation, which are critical factors in anesthesia management. By focusing on patients aged 18-65 with an ASA classification of 1-3, the study seeks to enhance preoperative assessments and improve patient safety during surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 18-65 undergoing thoracic surgery with an ASA classification of 1-3.
Not a fit: Patients with a history of obstructive sleep apnea syndrome or previous head and neck surgery/radiotherapy may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to better identification of patients at risk for difficult airway management, ultimately improving surgical outcomes and patient safety.
How similar studies have performed: While the STOP-BANG questionnaire has been widely used in various settings, this specific application in predicting difficult intubation during thoracic surgery is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient undergoing thoracic surgery * 18-65 years old * ASA 1-3 Exclusion Criteria: * Having a history of obstructive sleep apnea syndrome, * Having a history of previous head and neck surgery/radiotherapy, * Patients who did not agree to participate in the study
Where this trial is running
Ankara, Keçiören
- Ankara Atatürk Sanatorium Training and Research Hospital — Ankara, Keçiören, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: Ali ALAGÖZ, professor — Ankara Ataturk Sanatorium Training and Research Hospital
- Study coordinator: Ali ALAGÖZ, professor
- Email: mdalagoz@gmail.com
- Phone: 5079193765
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.