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New breathing tube removal method may prevent oxygen drops after C-Sections

NCT ID NCT07251686

Symptom relief Sponsor: Medipol 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested two different methods of removing the breathing tube after a C-section under general anesthesia. 120 women took part to see which method helps keep oxygen levels stable. The goal is to reduce breathing problems right after surgery.

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

120 people

The number who actually took part.

Started

Sep 2025

Finished

Nov 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 45 years

Sex

Female participants only

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: * Adult female patients aged 18 to 45 years. * Scheduled for elective cesarean delivery under general anesthesia. * Ability to provide written informed consent Exclusion Criteria: * Exclusion criteria included patients participating in another study, * Patients refusing to participate, * Uncooperative patients, * Patients undergoing emergency surgery, * American Society of Anesthesiologists (ASA) Physical Status Classification \> 3, * Patients with chronic respiratory failure, obstructive sleep apnea, and patients with anticipated difficult airways.

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Conditions

The condition(s) this trial relates to.

Hypoxia middle lobe syndrome Pulmonary Atelectasis

As listed by the trial registrant

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

Anesthesia, general Atelectasis Extubation Hypoxia Postoperative respiratory complication

Contacts and locations

Locations

  • Istanbul Medipol Mega University Hospital

    Istanbul, Bagcılar, Turkey (Türkiye)

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