Health Trials

Undiluted and Diluted Nutrition

ConditionsCritical IllnessGastro Intestinal SurgeryEnteral Feeding IntoleranceGastro-Intestinal DisorderQuality of Lifte
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohn Paul II Catholic University of Lublin

About this trial

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.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Enteral fluid
  • Intravenous fluid

Treatment groups

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators

John Paul II Catholic University of Lublin

Lead sponsor

Center of Oncology of the Lublin Region

Collaborator

Provincial Specialist Hospital in Lublin

Collaborator

Source ClinicalTrials.gov