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Which anesthesia helps you wake up faster after surgery?

NCT ID NCT07016308

Knowledge-focused Sponsor: Harran University 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 how two different anesthesia gases affect the body and recovery in 40 adults having ear, nose, or throat surgery. Researchers measured heart rate, blood pressure, oxygen levels, and how quickly patients woke up after surgery. The goal was to see if one gas leads to a smoother recovery than the other.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

40 people

The number who actually took part.

Started

Jun 2025

Finished

Dec 2025

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.

Ages

18 to 65 years

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 between 18 and 65 years * Classified as ASA physical status I or II * Scheduled to undergo elective ENT surgery (rhinoplasty, mastoidectomy, or tympanoplasty) * Requiring general anesthesia with endotracheal intubation * Providing written informed consent Exclusion Criteria: * ASA physical status III or higher * History of malignant hyperthermia or delayed emergence from anesthesia * Morbid obesity (BMI ≥ 35) * Coronary artery disease, congestive heart failure, COPD, liver or kidney disease * Pregnancy or breastfeeding * Allergy to halogenated anesthetics * Respiratory pathology * Substance or alcohol abuse

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As listed by the trial registrant

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

Anesthesia, general

Contacts and locations

Locations

  • Veli Fahri Pehlivan

    Sanliurfa, 63100, Turkey (Türkiye)

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