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Undiluted and Diluted Nutrition

NCT07352150 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-01-20

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 to assess feeding intolerance in both patient groups.

Conditions

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

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

  • Center of Oncology of the Lublin Region

    collaborator UNKNOWN

  • Provincial Specialist Hospital in Lublin

    collaborator UNKNOWN

  • John Paul II Catholic University of Lublin

    lead OTHER

Principal Investigators

  • Michał Borys · Medical Faculty, John Paul II Catholic University of Lublin

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-02
Primary Completion
2027-06-30
Completion
2027-09-30

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 NCT07352150 on ClinicalTrials.gov