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Sleep study after nose surgery cancelled before starting

NCT ID NCT07325799

Knowledge-focused Sponsor: Elazıg Fethi Sekin Sehir Hastanesi Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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
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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 was designed to see if the type of anesthesia used during nose surgery (septoplasty) affects how well patients sleep afterward. It planned to follow adults having surgery and ask about their sleep, pain, and nausea. However, the study was withdrawn before enrolling any participants, so no results are available.

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.

Started

Dec 2025

Expected to finish

Mar 2026

An estimate. End dates often move.

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 will consist of adult patients aged 18 years and older who are scheduled to undergo elective septoplasty under general anesthesia. Patients will receive either total intravenous anesthesia or inhalational anesthesia according to routine clinical practice. Only patients who provide written informed consent and agree to postoperative follow-up assessments will be included. The study population will be recruited from a single tertiary care hospital.

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: * \- 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

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As listed by the trial registrant

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

Inhalational anesthesia Nasal septum deviation Postoperative sleep quality Septoplasty Total intravenous anesthesia

Contacts and locations

Locations

  • Elazığ Fethi Sekin City Hospital

    Elâzığ, Merkez, 23200, Turkey (Türkiye)

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