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Anesthesia breathing study: which setting protects lungs better?

NCT ID NCT07305129

Knowledge-focused Sponsor: HULYA TOPCU, MD 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 11, 2026 · Updated 4 times

Summary

This study looked at 40 adults having general anesthesia to compare two ways of helping them breathe: pressure-controlled and volume-controlled ventilation. The goal was to see which method keeps lungs working better during and right after surgery. Results help anesthesiologists choose the best breathing support for low-flow anesthesia.

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

40 people

The number who actually took part.

Started

Aug 2023

Finished

Dec 2023

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

Hitit University Erol Olçok Training and Research Hospital

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: \- age 18-65 years and American Society of Anesthesiologists (ASA) physical status I-II. Exclusion Criteria: * morbid obesity (BMI \> 35 kg/m²), * scoliosis or thoracic deformity, * restrictive or obstructive lung disease, * prior thoracic or upper abdominal surgery, * history of major thoracic trauma or congenital chest wall anomaly, * active smoking or chronic use of corticosteroids, * β-agonists, bronchodilators, or antihistamines, * anticipated difficult airway * severe hypoxemia (SpO₂ \< 90%) during induction.

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As listed by the trial registrant

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

Asa class I/II patients General anesthetic Low flow anesthesia

Contacts and locations

Locations

  • Hitit University Erol Olçok Training and Research Hospital

    Çorum, Çorum, 19030, Turkey (Türkiye)

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