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Which anesthesia is safer for mom and baby during C-Section?

NCT ID NCT07513870

Knowledge-focused 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compared two types of general anesthesia—total intravenous anesthesia (TIVA) using propofol and inhalational anesthesia using sevoflurane—in 80 women having planned C-sections. Researchers measured how well each method controlled the mother's vital signs and the baby's neurological adaptation right after birth. The goal was to find which approach offers better safety and stability for both.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Propofol and sevoflurane
What this could lead to
If one method proves safer or more stable for mother and baby, it could become the preferred anesthesia approach for elective C-sections.
What could go wrong
This is a small, completed trial with only 80 participants. Results may not apply to emergency C-sections or women with other health conditions.

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

80 people

The number who actually took part.

Started

Mar 2024

Finished

Jan 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.

Ages

21 to 41 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: * Pregnant women scheduled for elective cesarean section under general anesthesia. * Gestational age of 38 weeks or greater. * American Society of Anesthesiologists (ASA) physical status II. Exclusion Criteria: * Emergency cesarean section (Category 1 and 2). * Presence of fetal distress. \* ASA physical status III or higher. * Preference for regional anesthesia. * Antenatally detected fetal anomalies. * Multiple pregnancies. * Estimated birth weight less than 2400 grams. * Known allergy to the study drugs or intraoperative adverse drug reactions. * Severe eclampsia. * Patients requiring conversion to general anesthesia due to inadequate spinal block.

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As listed by the trial registrant

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

Anesthesia, general Anesthesia, intravenous Cesarean section

Contacts and locations

Locations

  • Istanbul Medipol University

    Istanbul, Turkey (Türkiye)

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