Anesthesia Type and Postoperative Sleep Quality in Septoplasty
Evaluation of the Association Between Anesthesia Type and Postoperative Sleep Quality in Septoplasty Patients: A Prospective Observational Study
Elazıg Fethi Sekin Sehir Hastanesi
72 participants
Dec 1, 2025
OBSERVATIONAL
Conditions
Summary
This prospective observational study aims to evaluate the association between routinely applied anesthesia techniques and postoperative sleep quality in adult patients undergoing septoplasty. Patients will receive either total intravenous anesthesia or inhalational anesthesia according to standard clinical practice, without any intervention by the investigators. Postoperative sleep quality will be assessed using the Richards-Campbell Sleep Questionnaire on postoperative days 7 and 15. Secondary outcomes include postoperative pain intensity, opioid consumption, and postoperative nausea and vomiting.
Eligibility
Inclusion Criteria5
- \- Adults aged 18 years and older
- American Society of Anesthesiologists (ASA) physical status I-III
- Scheduled for elective septoplasty under general anesthesia
- Willing and able to provide written informed consent
- Agree to postoperative follow-up telephone interviews on postoperative days 7 and 15
Exclusion Criteria9
- \- ASA physical status IV or V
- Age younger than 18 years
- Severe obstructive sleep apnea confirmed by polysomnography and requiring active CPAP therapy
- Significant cognitive impairment, delirium, or active psychiatric disorder preventing reliable questionnaire completion
- Chronic use of opioids, benzodiazepines, hypnotics, sedatives, or antipsychotic medications (≥3 days per week within the last month)
- Alcohol or substance abuse
- Major intraoperative complications, unplanned intensive care unit admission, or reoperation within the first 24 hours
- Pregnancy or breastfeeding
- Severe systemic disease or unstable cardiopulmonary condition
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Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07325799