Clinical Trial

Anesthesia Type and Postoperative Sleep Quality in Septoplasty

Study acronym: ANES-SLEEP
Withdrawn
View on ClinicalTrials.gov →
Why the trial stopped
This record is a duplicate entry created in error. The correct study is registered under NCT07416773. The study was never initiated.
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.
Protocol Amendment History 2 changes
critical Trial status changed: Recruiting → Withdrawn 2026-04-25
notable Enrollment reduced: 72 -> 0 participants 2026-04-25
Trial Details
NCT Number NCT07325799
Lead Sponsor Elazıg Fethi Sekin Sehir Hastanesi
Conditions Postoperative Sleep Quality, Nasal Septum Deviation, Septoplasty, Total Intravenous Anesthesia, Inhalational Anesthesia
Start Date 2025-12-01
Primary Completion 2026-03-01 (estimated)
Study Completion 2026-03-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-24