Enteral Versus Parenteral Nutrition During Recovery After Shock
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19+
SponsorSamsung Medical Center
About this trial
This study compares enteral nutrition and parenteral nutrition in critically ill adult patients recovering from shock while receiving decreasing doses of vasopressors in the intensive care unit.
Eligible patients will be randomly assigned to receive either enteral or parenteral nutrition during the early recovery phase of shock.
The study aims to determine whether enteral nutrition improves clinical outcomes, including ICU mortality and ICU-acquired infections, compared with parenteral nutrition.
Eligibility criteria
Qualifiers
Subjects must be at least 19 years of age at the time of screening.
Subjects must be admitted to the intensive care unit (ICU).
Subjects must be receiving vasopressor therapy for shock.
Subjects must meet all screening criteria.
Disqualifiers
Subjects with contraindications to enteral nutrition (EN) or parenteral nutrition (PN) at the time of enrollment will be excluded.
Subjects requiring specific nutritional management, including but not limited to long-term home enteral nutrition, long-term parenteral nutrition, or a diagnosis of refeeding syndrome, will be excluded.
Subjects who are pregnant or breastfeeding will be excluded.
Subjects with severe comorbid conditions associated with an estimated life expectancy of less than three months will be excluded.
Trial design
Treatments tested in this trial
- enteral nutrition
- Parenteral Nutrition
Treatment groups
1,150 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov