Evaluation of Preoperative Gastric Ultrasonography in Pediatric Patients in Terms of Patient Safety
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-18
SponsorTC Erciyes University
About this trial
Preoperative evaluation of stomach fullness with ultrasound in children who will undergo anesthesia outside the operating room
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Children between 0-18 years of age and ASA I-II patients will be included in the study.
Disqualifiers
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,
Trial population
ASA I-II children aged 0-18 years who underwent non-operating room anesthesia
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
200 Participants
are grouped into 1 trial groupGroup A: Group undergoing gastric ultrasound
Trial outcomes
Primary outcomes
1
Qualitative assessment of residual gastric fluid volume
Grade 0: Defined as no contents visible in the antrum, the stomach is empty and the volume of the contents approaches zero. Grade 1: Visible clear fluid with a fluid volume of \<1.5 mL/kg. Grade 2: Defined as visible clear fluid with a fluid volume of \>1.5 mL/kg in both the supine and lateral decubitus positions.
Time frame
preoperative evaluation in the operating roomSecondary outcomes
1
Gastric content volume
It will be calculated using a mathematical model validated in children aged 11 months to 18 years. Volume(mL/kg) = \[-7.8 + 0.035 × antral area measured in lateral decubitus position (mm2) + 0.127 × age (months)\] / body weight (kg). The R² value for this model was 0.60.
Time frame
preoperative evaluation in the operating room2
Antral cross-sectional area
In both supine and lateral decubitus positions, between antral contractions, serosa to serosa, measuring the length diameter (D1) and the anteroposterior diameter (D2); Antral area = (π × D1 × D2) / 4 will be measured using the formula.
Time frame
preoperative evaluation in the operating roomSponsors and contacts
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Source ClinicalTrials.gov