Bedside Observation by Clinical Ultrasound for Stomach Expansion
Recruiting
N/A
Interventional Study
Enteral Feeding Intolerance
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 150 (estimated)
- Sponsor
- Centre Hospitalier Saint Joseph Saint Luc de Lyon · Other
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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.
Trial Locations
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Eligibility Criteria
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
Ex…
Contacts
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