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Sleep secrets after nose surgery: Anesthesia's surprising role revealed

NCT ID NCT07416773

Knowledge-focused Sponsor: Sevim Şenol Karataş Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 72 adults having nose surgery (septoplasty) to see if the type of anesthesia they received affected their sleep afterward. Patients got either total intravenous or inhalational anesthesia as part of their normal care. Researchers called them 7 and 15 days after surgery to ask about sleep quality, pain, and nausea.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

72 people

The number who actually took part.

Started

Nov 2025

Finished

Mar 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population consists of adult patients aged 18 years and older who undergo elective septoplasty at Elazig Fethi Sekin City Hospital. Eligible participants are classified as American Society of Anesthesiologists (ASA) physical status I-III and receive either total intravenous anesthesia or inhalational anesthesia as part of routine clinical care. Patients are enrolled consecutively after providing written informed consent, and no intervention or modification to standard anesthetic or postoperative management is performed as part of the study.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * • American Society of Anesthesiologists (ASA) Class I-III * Patients aged 18 and over * Those who provided written informed consent at the preoperative anesthesia clinic and allowed telephone follow-up on days 2/8. Exclusion Criteria: * • ASA Class IV and V * Patients under 18 years of age * Treatment of severe sleep disorders: Those with severe OSA confirmed by polysomnography and using active CPAP therapy. • Significant cognitive impairment, delirium, active psychotic disorder that prevents reliable completion of scales. • Regular use of hypnotics/benzodiazepines, sedatives/antipsychotics, or chronic opioids (≥3 days/week in the last month), alcohol or substance abuse. • Perioperative complications: Major complications during surgery, unplanned need for intensive care, or reoperation within the first 24 hours. • Pregnancy or breastfeeding. • Severe systemic disease, unstable cardiopulmonary status.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anesthesia techniques Postoperative sleep quality Septal deviation

Contacts and locations

Locations

  • Fethi Sekin City Hospital

    Elâzığ, Elaziğ, Turkey (Türkiye)

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