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Clinical Trials/NCT03699371
NCT03699371
Unknown
Not Applicable

Influence of Early vs Late Supplemental ParenteraL Nutrition on Long-term Quality of Life in ICU Patients After Gastrointestinal Oncological Surgery. A Prospective, Randomised, Multi-centre Assessor-blinded Study. hELPLiNe Trial

Medical University of Lublin2 sites in 1 country220 target enrollmentNovember 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nutrition Aspect of Cancer
Sponsor
Medical University of Lublin
Enrollment
220
Locations
2
Primary Endpoint
Long-term quality of life at 3 months
Last Updated
7 years ago

Overview

Brief Summary

BACKGROUND: Nutrition plays a significant role in ICU treatment, and may influence mortality and length of stay in ICU. Enteral route (EN) is preferential to parenteral route (PN) in provision of daily nutritional requirements. When enteral route is insufficient, supplemental parenteral nutrition (SPN) is recommended. Optimal timing of SPN in acute phase of illness remains elusive. ICU patients suffer significant lean body mass loss, in majority, in the first 7-10 days of stay. Optimal provision of protein may prevent muscle wasting. Lean body mass is essential for optimal physical functioning after treatment. Although ICU mortality has been reduced lately, the number of patients going to rehabilitation after ICU stay has tripled. Patients after oncological surgery of the gastrointestinal tract may be threatened with impairment of physical functioning after ICU treatment.

AIM: To compare the influence of early and late supplemental parenteral nutrition on long-term physical functioning in ICU patients after oncological surgery of the gastrointestinal tract.

STUDY DESIGN: Prospective, randomised, multi-centre assessor-blinded study. METHODS & ANALYSIS: Patients will be randomised into intervention group that would receive SPN on first day, and would be continued until 7th day of stay in ICU. Control group would receive SPN on 7th day of stay in ICU, when it is not then already met via enteral route. Physical Component of SF-36 Scale at 6 month after ICU admission will be assessed.

Registry
clinicaltrials.gov
Start Date
November 1, 2018
End Date
May 1, 2021
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Paweł Piwowarczyk

Principal Investigator

Medical University of Lublin

Eligibility Criteria

Inclusion Criteria

  • ICU patients in the acute phase of critical illness after gastrointestinal oncological surgery.
  • Admitted to the ICU during the previous 24 hours with a minimum expected ICU stay of ≥5 days
  • Central venous access available for continuous infusion of the study drugs
  • Sequential Organ Failure Assessment (SOFA) score ≥2
  • Written informed consent from the patient or the patient's legal representative

Exclusion Criteria

  • Contraindication against SPN or inability to receive SPN via central venous access
  • Received PN within 7 days before randomisation
  • Expected to receive ≥20% of energy via supplemental enteral nutrition (EN) and/or non-nutritional sources (e.g. glucose solution for drug dilution or lipids from propofol) during the first 3 nutritional treatment days
  • Inability to initiate EN prior to randomization
  • Body mass index (BMI) \<17 kg/m2 or \>35 kg/m2
  • Any severe, persistent blood coagulation disorder with uncontrolled bleeding
  • Any congenital errors of amino acid metabolism
  • Known hypersensitivity to fish, egg, soybean proteins, peanut proteins, or to any of the active substances or excipients contained in SPN.
  • Known hypersensitivity to milk protein or to any other substance contained in SPN
  • Acute liver failure with encephalopathy, including intoxication (e.g. paracetamol, death cap, golden chain) and/or liver enzymes (aspartate aminotransferase \[AST\], alanine aminotransferase \[ALT\], gamma glutamyl transferase \[GGT\]) or bilirubin exceeding 10 x ULN

Outcomes

Primary Outcomes

Long-term quality of life at 3 months

Time Frame: Physical component of 36 -SF questionnaire at 3 months after admission to ICU

Long-term quality of life measured in physical component of 36 -SF questionnaire

Long-term quality of life at 6 months

Time Frame: Physical component of 36 -SF questionnaire at 6 months after admission to ICU

Long-term quality of life measured in physical component of 36 -SF questionnaire

Secondary Outcomes

  • Insulin dose(For 7 days since admission to ICU)
  • Mechanical Ventilation(For 28 days since admission to ICU or till discharge)
  • Thickness of diaphragm(1st, 3rd, 5th day of ICU stay)
  • Protein delivery(For 7 days since admission to ICU)
  • Blood glucose profile(For 7 days since admission to ICU)
  • Organic phosphorus level(For 7 days since admission to ICU)
  • ICU mortality(For 28 days since admission to ICU or till discharge)
  • Hospital mortality(For 28 days since admission to ICU or till discharge)
  • Health-care associated infection(For 28 days since admission to ICU or till discharge)
  • Length of stay in the ICU(For 28 days since admission to ICU or till discharge)
  • Sequential Organ Failure Assessment score ( SOFA score)(For 28 days since admission to ICU or till discharge)
  • Length of stay in hospital(For 28 days since admission to ICU or till discharge)
  • Energy Intake(For 7 days since admission to ICU)
  • Antibiotic-free days(For 28 days since admission to ICU or till discharge)
  • Enteral route intolerance(At day 3 since admission to ICU)

Study Sites (2)

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