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A Randomized Controlled Study of Enteral Nutrition in Septic Shock

Primary Purpose

Septic Shock

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Enteral nutrition
Sponsored by
Medical College of Wisconsin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Septic Shock focused on measuring septic shock, mechanical ventilation, enteral nutrition, trophic feeding

Eligibility Criteria

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

Inclusion Criteria:

  • Adults greater than or equal to 18 years old
  • Clinical diagnosis of septic shock
  • Mechanically ventilation anticipated for at least 48 hours

Exclusion Criteria:

  • Do not resuscitate order
  • Not able to obtain consent
  • Those not able to be randomized within 18 hours
  • Those with small bowel ischemia or obstruction
  • Protracted ileus, intractable vomiting, major gastrointestinal bleeding defined as needing 2 or more units of packed red cells, and any bowel surgery within the previous 30 days prior to intensive care unit admission
  • Those with a contraindication for placement of a feeding tube

Sites / Locations

  • Froedtert Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Trophic feeding

No Enteral Nutrition

Arm Description

Mechanically ventilated patients with septic shock > 18 years old randomized to this group will receive more than 50 but less than 600 kilocalories of enteral nutrition per day while on vasopressors. This will be started within 24 hours of intensive care unit admission.

Mechanically ventilated patients with septic shock randomized to this group will receive no enteral nutrition while on vasopressor support.

Outcomes

Primary Outcome Measures

number of patients consenting to study and remaining compliant with assigned study arm
consent and compliance rate of >75% and contamination rate <10%

Secondary Outcome Measures

Ventilator free days
Number of days alive and off mechanical ventilatory support out of 30
Hospital mortality
number of patients who died during hospitalization
intensive care unit free days
number of days alive and out of the intensive care unit out of 30
change in 48 hour sequential organ failure assessment score, with higher score representing worse outcome
absolute change in sequential organ failure assessment score (range 0-24 points) from day 0 to 48 hours, with higher scores representing worse outcomes

Full Information

First Posted
December 17, 2013
Last Updated
August 13, 2019
Sponsor
Medical College of Wisconsin
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1. Study Identification

Unique Protocol Identification Number
NCT02025127
Brief Title
A Randomized Controlled Study of Enteral Nutrition in Septic Shock
Official Title
A Randomized Controlled Study of Enteral Nutrition in Septic Shock
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
January 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical College of Wisconsin

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
There is a paucity of data on the timing and role of enteral nutrition in septic shock. The primary aim of this study is to conduct a phase III single-center pilot randomized controlled trial comparing early trophic enteral nutrition to 'no enteral nutrition' in mechanically ventilated septic shock patients to determine feasibility.
Detailed Description
Septic shock represents the body's dysregulated response to an infection, manifesting as persistent hypotension (mean arterial pressure < 70 mmHg) despite intravenous (IV) fluid resuscitation. Severe sepsis and septic shock are major healthcare problems, affecting millions of people around the world each year In critically ill patients without shock, provision of enteral nutrition within 24-48 hours has shown to preserve intestinal epithelium, maintain brush border enzyme activity, maintenance of barrier function to enhance immune function, and preservation of tight cell junctions to reduce permeability. These benefits of enteral nutrition are postulated to prevent downstream complications of nosocomial infections and the multiple organ dysfunction syndrome (MODS), though direct data addressing this question are lacking. The primary aim of this study is to conduct a phase III single-center pilot randomized controlled trial comparing early trophic EN to 'no EN' in mechanically ventilated septic shock patients to determine feasibility of achieving >75% consent and compliance rate and <10% contamination rate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock
Keywords
septic shock, mechanical ventilation, enteral nutrition, trophic feeding

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Trophic feeding
Arm Type
Experimental
Arm Description
Mechanically ventilated patients with septic shock > 18 years old randomized to this group will receive more than 50 but less than 600 kilocalories of enteral nutrition per day while on vasopressors. This will be started within 24 hours of intensive care unit admission.
Arm Title
No Enteral Nutrition
Arm Type
No Intervention
Arm Description
Mechanically ventilated patients with septic shock randomized to this group will receive no enteral nutrition while on vasopressor support.
Intervention Type
Other
Intervention Name(s)
Enteral nutrition
Intervention Description
Enteral nutrition introduced via a feeding tube
Primary Outcome Measure Information:
Title
number of patients consenting to study and remaining compliant with assigned study arm
Description
consent and compliance rate of >75% and contamination rate <10%
Time Frame
46 months
Secondary Outcome Measure Information:
Title
Ventilator free days
Description
Number of days alive and off mechanical ventilatory support out of 30
Time Frame
30 days
Title
Hospital mortality
Description
number of patients who died during hospitalization
Time Frame
30 days
Title
intensive care unit free days
Description
number of days alive and out of the intensive care unit out of 30
Time Frame
30 days
Title
change in 48 hour sequential organ failure assessment score, with higher score representing worse outcome
Description
absolute change in sequential organ failure assessment score (range 0-24 points) from day 0 to 48 hours, with higher scores representing worse outcomes
Time Frame
48 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults greater than or equal to 18 years old Clinical diagnosis of septic shock Mechanically ventilation anticipated for at least 48 hours Exclusion Criteria: Do not resuscitate order Not able to obtain consent Those not able to be randomized within 18 hours Those with small bowel ischemia or obstruction Protracted ileus, intractable vomiting, major gastrointestinal bleeding defined as needing 2 or more units of packed red cells, and any bowel surgery within the previous 30 days prior to intensive care unit admission Those with a contraindication for placement of a feeding tube
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jayshil J Patel, MD
Organizational Affiliation
Medical College of Wisconsin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Froedtert Hospital
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
15639681
Citation
Annane D, Bellissant E, Cavaillon JM. Septic shock. Lancet. 2005 Jan 1-7;365(9453):63-78. doi: 10.1016/S0140-6736(04)17667-8.
Results Reference
background
PubMed Identifier
23361625
Citation
Dellinger RP, Levy MM, Rhodes A, Annane D, Gerlach H, Opal SM, Sevransky JE, Sprung CL, Douglas IS, Jaeschke R, Osborn TM, Nunnally ME, Townsend SR, Reinhart K, Kleinpell RM, Angus DC, Deutschman CS, Machado FR, Rubenfeld GD, Webb S, Beale RJ, Vincent JL, Moreno R; Surviving Sepsis Campaign Guidelines Committee including The Pediatric Subgroup. Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock, 2012. Intensive Care Med. 2013 Feb;39(2):165-228. doi: 10.1007/s00134-012-2769-8. Epub 2013 Jan 30.
Results Reference
background
PubMed Identifier
19398613
Citation
McClave SA, Martindale RG, Vanek VW, McCarthy M, Roberts P, Taylor B, Ochoa JB, Napolitano L, Cresci G; A.S.P.E.N. Board of Directors; American College of Critical Care Medicine; Society of Critical Care Medicine. Guidelines for the Provision and Assessment of Nutrition Support Therapy in the Adult Critically Ill Patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.). JPEN J Parenter Enteral Nutr. 2009 May-Jun;33(3):277-316. doi: 10.1177/0148607109335234. No abstract available.
Results Reference
background
PubMed Identifier
18849555
Citation
Cresci G, Cue J. The patient with circulatory shock: to feed or not to feed? Nutr Clin Pract. 2008 Oct-Nov;23(5):501-9. doi: 10.1177/0884533608323431.
Results Reference
background
PubMed Identifier
11355123
Citation
Revelly JP, Tappy L, Berger MM, Gersbach P, Cayeux C, Chiolero R. Early metabolic and splanchnic responses to enteral nutrition in postoperative cardiac surgery patients with circulatory compromise. Intensive Care Med. 2001 Mar;27(3):540-7. doi: 10.1007/s001340100855.
Results Reference
background
PubMed Identifier
20436064
Citation
Khalid I, Doshi P, DiGiovine B. Early enteral nutrition and outcomes of critically ill patients treated with vasopressors and mechanical ventilation. Am J Crit Care. 2010 May;19(3):261-8. doi: 10.4037/ajcc2010197. Erratum In: Am J Crit Care. 2010 Nov;19(6):488.
Results Reference
background
PubMed Identifier
1303622
Citation
Bone RC, Balk RA, Cerra FB, Dellinger RP, Fein AM, Knaus WA, Schein RM, Sibbald WJ. Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis. The ACCP/SCCM Consensus Conference Committee. American College of Chest Physicians/Society of Critical Care Medicine. Chest. 1992 Jun;101(6):1644-55. doi: 10.1378/chest.101.6.1644.
Results Reference
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A Randomized Controlled Study of Enteral Nutrition in Septic Shock

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