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The PREServation of MUScle Function in Critically Ill Patients (PRESMUS) (PRESMUS)

Primary Purpose

Critically Ill

Status
Unknown status
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Whey protein supplement
Sponsored by
Amsterdam UMC, location VUmc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Critically Ill focused on measuring Critical care, nutrition, whey protein, mechanical ventilation, muscle function

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Admitted to the intensive care
  • Mechanically ventilated
  • Expected duration of ventilation of 72 hours
  • Expected to tolerate and require enteral nutrition for more than 72 hours
  • Sequential organ failure assessment (SOFA)-score>6 on admission day
  • Written informed consent of patient or legal representative

Exclusion Criteria:

  • Contra-indication to enteral nutrition
  • Short bowel syndrome
  • Child C liver cirrhosis or acute liver failure
  • Dialysis dependency
  • Requiring other specific enteral nutrition for medical reason
  • Body mass index (BMI) > 35 kg/m2
  • Extensive treatment limitations
  • Disseminated malignancy
  • Haematological malignancy
  • Primary neuromuscular pathology
  • Chronic use of corticosteroids for > 7 days before ICU admission
  • Contra-indication for muscle biopsy (need for uninterrupted systemic anticoagulation, prothrombin time >1.4 , Thrombocytes <100).

Sites / Locations

  • VU Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

intervention group

control group

Arm Description

whey protein supplement enriched enteral nutrition, with protein intake of 1.5g/kg/day; in addition to standardized exercise training

standard enteral nutrition, with protein intake of 1g/kg/day; in addition to standardized exercise training

Outcomes

Primary Outcome Measures

in vitro loss of skeletal muscle function
measured by contractility of of individual muscle fibers

Secondary Outcome Measures

loss of muscle function
Medical research council (MRC) sum score,
changes in body composition
Bioelectrical impedance analysis (BIA)
loss of muscle mass
Ultrasound (US) of the quadriceps femoris muscle and diaphragm, questionnaires
quality of life
Short form (SF)- 36 questionnaire

Full Information

First Posted
April 21, 2017
Last Updated
July 26, 2017
Sponsor
Amsterdam UMC, location VUmc
Collaborators
Société des Produits Nestlé (SPN)
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1. Study Identification

Unique Protocol Identification Number
NCT03231540
Brief Title
The PREServation of MUScle Function in Critically Ill Patients (PRESMUS)
Acronym
PRESMUS
Official Title
Effect of Whey Protein-enriched Enteral Nutrition in Addition to Standardized Exercise Training on the PREServation of MUScle Function in Critically Ill Patients: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2016 (undefined)
Primary Completion Date
September 2018 (Anticipated)
Study Completion Date
September 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Amsterdam UMC, location VUmc
Collaborators
Société des Produits Nestlé (SPN)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study evaluates the effect of whey protein enriched enteral nutrition in addition to exercise training on the preservation of muscle function in critically ill patients. One half of patients receive whey protein enriched enteral nutrition with a protein intake of 1.5 g/kg/day and the other half of patients receive standard enteral nutrition with a protein intake of 1 g/kg/day.
Detailed Description
Muscle wasting has an enormous impact on long-term physical performance and quality of life of intensive care survivors. Limitation of muscle wasting might therefore improve physical performance and quality of life. Data on high protein nutritional intake in addition to a standardized exercise training program to prevent skeletal muscle wasting during critical illness are lacking. Objective: to determine whether early high protein intake, using an enteral whey protein supplement, in addition to a standardized exercise training program and standard enteral nutrition preserves: a) in vitro skeletal muscle function in critically ill patients during the first week of intensive care unit (ICU) admission and b) short- and long-term in vivo muscle function and mass, clinical outcomes and quality of life in critically ill patients. Secondly, to determine whether high protein intake, in addition to standardized exercise and standard enteral nutrition, increases muscle protein synthesis and attenuates activation of the Ubiquitin-Proteasome pathway in critically ill patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critically Ill
Keywords
Critical care, nutrition, whey protein, mechanical ventilation, muscle function

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
intervention group
Arm Type
Experimental
Arm Description
whey protein supplement enriched enteral nutrition, with protein intake of 1.5g/kg/day; in addition to standardized exercise training
Arm Title
control group
Arm Type
No Intervention
Arm Description
standard enteral nutrition, with protein intake of 1g/kg/day; in addition to standardized exercise training
Intervention Type
Dietary Supplement
Intervention Name(s)
Whey protein supplement
Other Intervention Name(s)
Beneprotein Nestle
Intervention Description
Whey protein supplement to target protein intake of 1.5 g/kg/day
Primary Outcome Measure Information:
Title
in vitro loss of skeletal muscle function
Description
measured by contractility of of individual muscle fibers
Time Frame
day 1-3 and day 8-10
Secondary Outcome Measure Information:
Title
loss of muscle function
Description
Medical research council (MRC) sum score,
Time Frame
day 1-3, day 8-10, day 28
Title
changes in body composition
Description
Bioelectrical impedance analysis (BIA)
Time Frame
day 1-3, day 8-10, day 28
Title
loss of muscle mass
Description
Ultrasound (US) of the quadriceps femoris muscle and diaphragm, questionnaires
Time Frame
day 1-3, day 8-10, day 28
Title
quality of life
Description
Short form (SF)- 36 questionnaire
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admitted to the intensive care Mechanically ventilated Expected duration of ventilation of 72 hours Expected to tolerate and require enteral nutrition for more than 72 hours Sequential organ failure assessment (SOFA)-score>6 on admission day Written informed consent of patient or legal representative Exclusion Criteria: Contra-indication to enteral nutrition Short bowel syndrome Child C liver cirrhosis or acute liver failure Dialysis dependency Requiring other specific enteral nutrition for medical reason Body mass index (BMI) > 35 kg/m2 Extensive treatment limitations Disseminated malignancy Haematological malignancy Primary neuromuscular pathology Chronic use of corticosteroids for > 7 days before ICU admission Contra-indication for muscle biopsy (need for uninterrupted systemic anticoagulation, prothrombin time >1.4 , Thrombocytes <100).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sandra N Stapel, MD
Email
s.stapel@vumc.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Monique Waard
Email
mc.dewaard@vumc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sandra N Stapel, MD
Organizational Affiliation
Amsterdam UMC, location VUmc
Official's Role
Principal Investigator
Facility Information:
Facility Name
VU Medical Center
City
Amsterdam
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandra Stapel, M.D.

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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The PREServation of MUScle Function in Critically Ill Patients (PRESMUS)

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