Bedside Observation by Clinical Ultrasound for Stomach Expansion

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Saint Joseph Saint Luc de Lyon

About this trial

The objective of the BOCUSE study is to demonstrate a relationship between an early ultrasound measurement of the gastric antral area and the subsequent occurrence of poor gastric tolerance.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Predicted mechanical ventilation ≥ 48 hours

Initiation of enteral nutrition via nasogastric or orogastric tube for ≥ 48 hours

Free and informed consent obtained from the patient's relative or legal representative, or inclusion in an emergency situation

Disqualifiers

History of major gastric surgery (bypass, total gastrectomy, biliopancreatic diversion)

Enteral nutrition via nasogastric or orogastric tube > 96 hours

Initiation of enteral nutrition before intubation

Feeding via gastrostomy, jejunostomy, or jejunal tube

Trial design

Treatments tested in this trial

  • Gastric ultrasound with measurement of the antral area

Treatment groups

150 Participants
are divided into 1 treatment group