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Diluted and Undiluted Enteral Nutrition

StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Study description expanded, about 1 wordv2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Adult patients after elective major abdominal surgeries who are planned to be admitted to the Intensive Care Unit (ICU) can be included in the trial. Each patient will be fed via the gastrointestinal tract. Half of the patients will receive enteral nutrition (EN) with additional fluids, and the rest will receive undiluted EN. The primary aim of this study is feeding intolerance assessment in both groups of patients.
Trial Details
NCT Number NCT06516835
Lead Sponsor Medical University of Lublin
Collaborators: Nutricia Fundation, Catholic University of Lublin
Conditions
(from sponsor)		 Critical Illness, Surgery, Enteral Feeding Intolerance, Gastro-Intestinal Disorder, Quality of Life
Related terms Critical Illness, Digestive System Diseases, Ketosis
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov