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Effect of Resuscitation on Gastric Emptying Using POCUS in Pediatric Trauma Patients

Effect of Resuscitation on Gastric Emptying by Gastric Residual Volume Assessment Using Point of Care Ultrasonography in Pediatric Trauma Patients

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07810907
Enrollment
50
Registered
2026-09-09
Start date
2026-10-01
Completion date
2027-11-01
Last updated
2026-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delayed Gastric Emptying, Gastric Dysmotility, Hemorrhagic Shock, Pediatric Trauma

Keywords

Point-of-Care Ultrasound (POCUS), Gastric Residual Volume, Gastric Antral Cross-Sectional Area, Hemodynamic Resuscitation, Pulmonary Aspiration Risk, Pediatric Emergency Medicine

Brief summary

Pediatric trauma often leads to hemorrhagic shock, which reduces blood flow to the digestive tract and delays gastric emptying. This delay can cause fluid and food to remain in the stomach, increasing the risk of pulmonary aspiration during urgent airway management or emergency anesthesia. Point-of-care ultrasound (POCUS) is a bedside, non-invasive tool that allows clinicians to evaluate stomach contents and estimate gastric volume in real time. The primary purpose of this study is to evaluate whether restoring systemic blood flow through hemodynamic resuscitation improves gastric emptying and decreases gastric residual volume in injured children. Participants aged 2 to 7 years presenting to the emergency department with trauma and hemorrhagic shock will receive standard resuscitation according to pediatric advanced life support guidelines. Bedside gastric ultrasound will be performed to measure the antral cross-sectional area and calculate gastric residual volume before resuscitation begins, immediately following initial resuscitation, and every 6 hours for up to 48 hours. Ultrasound procedures are observational and will not delay any standard trauma care or urgent surgical interventions.

Interventions

None listed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 7 Years

Inclusion criteria

* Pediatric patients aged 2 to 7 years presenting with trauma. * Presenting with hemorrhagic shock requiring hemodynamic resuscitation (diagnosed according to Advanced Paediatric Life Support \[APLS\] guidelines based on clinical and laboratory evidence of inadequate tissue perfusion secondary to acute blood loss, such as age-adjusted hypotension, tachycardia, prolonged capillary refill time \> 2 seconds, weak peripheral pulses, altered mental status, elevated serum lactate, and/or increased base deficit). * Hemodynamically stable enough to undergo point-of-care gastric ultrasound (POCUS) examination without delaying emergency medical management.

Exclusion criteria

* Known gastrointestinal diseases affecting gastric motility (e.g., gastric outlet obstruction, intestinal obstruction). * History of prior upper gastrointestinal surgery. * Significant abdominal injury that may affect gastric motility. * Need for immediate emergency surgical intervention before completion of study baseline assessments. * Inability to adequately perform gastric POCUS (e.g., extensive abdominal wounds, surgical emphysema, or poor acoustic window). * Gastric decompression performed before the initial ultrasound assessment. * Isolated head injury.

Design outcomes

Primary

MeasureTime frameDescription
Change in Gastric Residual Volume (GRV)Baseline, Up to 4 HoursChange in gastric residual volume (mL/kg) from pre-resuscitation baseline to immediately after completion of hemodynamic resuscitation. Antral cross-sectional area (CSA) will be measured by point-of-care gastric ultrasound (POCUS) in the right lateral decubitus position (CSA = AP × CC × π/4), and gastric volume will then be estimated using the Spencer formula and normalized to body weight (mL/kg).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 10, 2026