Bedside Observation by Clinical Ultrasound for Stomach Expansion (NCT07312890) | Clinical Trial Compass
RecruitingNot Applicable
Bedside Observation by Clinical Ultrasound for Stomach Expansion
France150 participantsStarted 2025-10-25
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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
Exclusion Criteria:
* 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
* Pregnancy
* Prognosis considered terminal
* No ultrasound window available
* Legally protected adults (under curatorship, guardianship, or judicial protection)
* No social security coverage
* Patient under State Medical Aid (AME)
What they're measuring
1
Enteral nutrition intolerance
Timeframe: Within 7 days following the gastric ultrasound
Trial details
NCT IDNCT07312890
SponsorCentre Hospitalier Saint Joseph Saint Luc de Lyon