RecruitingNCT07325799

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


Sponsor

Elazıg Fethi Sekin Sehir Hastanesi

Enrollment

72 participants

Start Date

Dec 1, 2025

Study Type

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

Min Age: 18 Years

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

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Elazığ Fethi Sekin City Hospital

Elâzığ, Merkez, Turkey (Türkiye)

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07325799


Related Trials