Anesthesia Type and Postoperative Sleep Quality in Septoplasty (NCT07325799) | Clinical Trial Compass
WithdrawnNot Applicable
Anesthesia Type and Postoperative Sleep Quality in Septoplasty
Stopped: This record is a duplicate entry created in error. The correct study is registered under NCT07416773. The study was never initiated.
Turkey (Türkiye)0Started 2025-12-01
Plain-language 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.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* \- 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 Criteria:
* \- 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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Richards-Campbell Sleep Questionnaire (RCSQ) Total Score
Timeframe: Postoperative day 7 and postoperative day 15