Clinical Trial

Undiluted and Diluted Nutrition

Not Yet Recruiting
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Summary
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 to assess feeding intolerance in both patient groups.
Trial Details
NCT Number NCT07352150
Lead Sponsor John Paul II Catholic University of Lublin
Collaborators: Center of Oncology of the Lublin Region, Provincial Specialist Hospital in Lublin
Conditions Critical Illness, Gastro Intestinal Surgery, Enteral Feeding Intolerance, Gastro-Intestinal Disorder, Quality of Lifte
Enrollment 80 participants
Start Date 2026-02-02
Primary Completion 2027-06-30 (estimated)
Study Completion 2027-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-01-20