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Ultrasound study checks stomach safety of Pre-Surgery water in diabetic Moms-to-Be

NCT ID NCT07482098

Knowledge-focused Sponsor: Ankara City Hospital Bilkent Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 looks at whether drinking 200 ml of water two hours before a planned C-section changes stomach volume differently in pregnant women with diabetes compared to those without. Researchers will use ultrasound to measure stomach contents before and after drinking. The goal is to improve safety guidelines for fasting before anesthesia.

What this could mean

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

Active substance
200 ml of water
What this could lead to
If successful, this study could help doctors better assess aspiration risk and refine fasting guidelines for pregnant women with diabetes.
What could go wrong
This is a small observational study, not a treatment trial. Results may not apply to all pregnant women or change current practice without larger studies.

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

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Started

Dec 2025

Expected to finish

Jul 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

Pregnant women aged 18-40 years undergoing elective cesarean section under spinal anesthesia at a tertiary care hospital. The study includes both diabetic and non-diabetic pregnant women who meet the eligibility criteria and provide informed consent.

Ages

18 to 40 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 aged 18-40 years * Scheduled for elective cesarean section under spinal anesthesia * Singleton pregnancy * ASA physical status II * Patients who provide written informed consent Exclusion Criteria: * Refusal to participate in the study * Contraindication to spinal anesthesia * Known allergy to study medications * Multiple pregnancy * Severe systemic disease (ASA III or higher) * Pre-existing neurological disease * Infection at the spinal puncture site

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Conditions

The condition(s) this trial relates to.

aspiration pneumonia gestational diabetes

As listed by the trial registrant

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

Diabetes in pregnancy Pregnancy Pulmonary aspiration

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Ankara Bilkent City Hospital

    RECRUITING

    Ankara, Ankara, 06800, Turkey (Türkiye)

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