RecruitingNot Applicable

Evaluation of Preoperative Gastric Ultrasonography in Pediatric Patients in Terms of Patient Safety

Turkey (Türkiye)200 participantsStarted 2024-11-15

Plain-language summary

Preoperative evaluation of stomach fullness with ultrasound in children who will undergo anesthesia outside the operating room

Who can participate

Age range

0 Years – 18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Children between 0-18 years of age and ASA I-II patients will be included in the study. Exclusion Criteria: * Patients over 18 years of age, * ASA-III and above patients, * patients with gastrointestinal dysfunction, * patients who cannot assume the lateral decubitus position for gastric -ultrasound measurements, * those who have had previous lower esophageal or gastric surgery, * those who do not comply with institutional fasting guidelines, * those with concomitant systemic diseases affecting gastric emptying, * those with a high body mass index (BMI) \> 40 kg/m2, * those with gastroesophageal reflux or aspiration risk factors, and emergency cases with delayed gastric emptying despite appropriate fasting time will not be included in the study.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Qualitative assessment of residual gastric fluid volume

Timeframe: preoperative evaluation in the operating room

Trial details

NCT IDNCT07581691

SponsorTC Erciyes University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-07-31

Contact for this trial

Özlem OZ GERGIN, MD

09005332466396 oozgergin@erciyes.edu.tr

View on ClinicalTrials.gov More Nonoperating Room Anesthesia trials

Who can participate

Age range

0 Years – 18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.