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Anesthesia Type and Postoperative Sleep Quality in Septoplasty

NCT07325799 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2026-04-24

No results posted yet for this study

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.

Conditions

  • Postoperative Sleep Quality
  • Nasal Septum Deviation
  • Septoplasty
  • Total Intravenous Anesthesia
  • Inhalational Anesthesia

Sponsors & Collaborators

  • Elazıg Fethi Sekin Sehir Hastanesi

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-12-01
Primary Completion
2026-03-01
Completion
2026-03-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07325799 on ClinicalTrials.gov