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Diluted and Undiluted Enteral Nutrition

NCT06516835 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-07-26

No results posted yet for this study

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 feeding intolerance assessment in both groups of patients.

Conditions

  • Critical Illness
  • Surgery
  • Enteral Feeding Intolerance
  • Gastro-Intestinal Disorder
  • Quality of Life

Interventions

OTHER

Enteral fluid

GNAK will be administered to the gastrointestinal tract with EN in the same volume.

OTHER

Intravenous fluid

Undiluted EN will be given to the gastrointestinal tract. GNAK, in the same volume, will be administered intravenously.

Sponsors & Collaborators

  • Nutricia Fundation

    collaborator UNKNOWN

  • Catholic University of Lublin

    collaborator UNKNOWN

  • Medical University of Lublin

    lead OTHER

Principal Investigators

  • Michal Borys, MD, PhD · Medical University of Lublin

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-02
Primary Completion
2027-01-31
Completion
2027-04-30

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06516835 on ClinicalTrials.gov