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New study tests sips before surgery to calm Kids' nerves

NCT ID NCT07482345

Symptom relief Sponsor: Bursa City Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 20, 2026 · Updated 2 times

Summary

This study will test three different fasting plans in 90 children having groin or genital surgery. One group will follow traditional fasting, another will get a carbohydrate drink two hours before surgery, and a third will be allowed small sips of clear fluids until they go to the operating room. Researchers will measure anxiety levels and use ultrasound to check stomach contents, aiming to find a safer and more comfortable approach.

What this could mean

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

Active substance
clear apple juice and water
What this could lead to
If successful, this could lead to more comfortable and less stressful fasting guidelines for children before surgery.
What could go wrong
This is a small, early-stage trial with only 90 children, so results may not apply to all surgeries or hospitals. The study hasn't started yet.

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

About 90 people

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

Started

Mar 2026

Expected to finish

Apr 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

2 to 12 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: * Patients scheduled to undergo elective surgery under general anesthesia for circumcision, undescended testis, inguinal hernia, and/or hypospadias (inguinoscrotal surgery) * Patients with an ASA physical status classification of I-II * Patients able to tolerate oral intake in the preoperative period and comply with the assigned fasting protocol * Written informed consent obtained from parents or legal guardians Exclusion Criteria: * Patients with ASA physical status III or higher * Patients requiring emergency surgery * History of gastroesophageal reflux disease, gastrointestinal motility disorders, or metabolic/neurological diseases affecting gastric emptying * History of upper gastrointestinal surgery * Active upper respiratory tract infection or lower respiratory tract infection within the previous 2-4 weeks * Severe pulmonary disease, including uncontrolled or moderate-to-severe persistent asthma, bronchopulmonary dysplasia, cystic fibrosis, interstitial lung disease, or other chronic lung diseases * Diabetes mellitus or endocrine/metabolic disorders that may affect perioperative glucose metabolism * Obese patients with high aspiration risk (\>95th percentile for age) * Cognitive or communication impairments that may interfere with compliance with the study protocol * Grade 2 or Grade 3 gastric fullness detected on preoperative gastric ultrasonography * Lack of written informed consent from parents or legal guardians for participation in the study

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As listed by the trial registrant

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

Enhanced recovery after surgery (ERAS) protocol Pediatric surgery Preoperative fasting

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

  • University of Health Sciences, Bursa City Hospital

    ACTIVE_NOT_RECRUITING

    Bursa, Bursa, 16110, Turkey (Türkiye)

  • University of Health Sciences, Bursa City Hospital

    RECRUITING

    Bursa, Nilufer, 16110, Turkey (Türkiye)

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