ConditionEnteral Feeding Intolerance
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 groupSponsors and collaborators
Source ClinicalTrials.gov