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Intermittent Versus Continuous Enteral Nutrition in Mechanically Ventilated Patients in the Medical Intensive Care Unit

Primary Purpose

Enteral Feeding, Nutrition Disorders

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Intermittent feed participant
Continuous feeds participant
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Enteral Feeding

Eligibility Criteria

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

INCLUSION CRITERIA

  • MICU Yale New Haven Hospital
  • Age >= 18 years old.
  • Patients mechanically ventilated via endotracheal tube
  • Patients intubated within 72 hours of hospital admission
  • First intubation of current hospitalization
  • First MICU admission of current hospitalization

EXCLUSION CRITERIA

• Patient has opted out of research participation via institutional patient portal.

At significant risk for gastrointestinal intolerance of intermittent bolus feeds:

  • Prior upper gastrointestinal surgery that alters proximal GI anatomy (including but not limited to gastric bypass surgery, gastric banding, complete or partial gastrectomy, Whipple procedure; of note, appendectomy and cholecystectomy are not exclusion criteria.
  • Structural gastrointestinal obstruction (such as tumor).
  • Chronic enteral nutrition (prior to current admission).
  • History of significant esophageal dysmotility (history of GERD is acceptable) or clinically significant GE junction incompetence
  • Unable to have head of bed elevated at least 30 degrees while intubated and being fed (this is standard protocol).
  • Enteral access terminates post-pyloric (ie nasojejunal or jejunostomy tubes are to be excluded) or unable to place gastric tube for access. (The clinical team will determine type of tube placement. As this is particularly selected by intensivists for patients at higher aspiration risk, this tube enteral access exclusion de facto excludes patients at high aspiration risk.)
  • History of small bowel obstruction or ileus on current admission or within last 1 month.
  • History of gastroparesis.
  • Percutaneous gastrostomy tube or tracheostomy.
  • History of ongoing aspiration as determined by a speech medicine specialist or other medical professional or a patent who required adjustment of diet (e.g., thickening of liquids) prior to hospitalization.
  • History of significant esophageal dysmotility (history of GERD is acceptable) or clinically significant GE junction incompetence

Other Exclusion Criteria:

  • At risk of refeeding syndrome.
  • Pregnant patients.
  • Patients receiving neuromuscular blockade.
  • Patients with glycemic emergency (HHNK, DKA, severe hypoglycemia resulting in MICU admission) or patients controlling their sugar / insulin dosing via continuous glucose monitoring
  • Post cardiac arrest (on current admission).
  • Received >= 6 hours of enteral nutrition (regardless of volume) at the time of screening and team is able to consent / enroll / initiate intermittent feed within an additional 2 hours.
  • Plan for extubation within 24 hours.
  • Not English-speaking.
  • Patients otherwise excluded by the treating physician.
  • Retrospective exclusion: patients who initially met eligibility criteria, but no nutrition consult (i.e., decision to initiate feeds by clinical providers) placed within 72 hours of intubation.

Sites / Locations

  • Yale New Haven Hospital, York Street CampusRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Intermittent feed

Continuous feeds

Arm Description

Patients will be assigned to receive intermittent enteral feeding protocol. They will receive four equal volume feeds at 8:00, 12:00, 16:00, and 20:00 hours.

Patients will be assigned to receive continuous enteral feeding protocol. Typical goal rates are in the range of 60 to 80 mL per hour for 24 hours per day.

Outcomes

Primary Outcome Measures

Recommended calories
percentage of recommended calories that patient receives per day of interest during study period

Secondary Outcome Measures

Percentage of patients with aspiration
percentage of patients experiencing aspiration
Percentage of patients experiencing intolerance of feeding
percentage of patients experiencing intolerance of feeding including nausea, vomiting, diarrhea, ileus
feasibility: proportion complete protocol
percentage of patients assigned to intervention (ie intermittent feeding protocol) that remain on study protocol for study period of interest.
delirium
number of delirium and coma free days out of 14 following intubation
urine 6-sulfatoxymelatonin acrophase
Urine 6-sulfatoxymelatonin acrophase defined as the time of fitted peak 6-sulfatoxymelatonin from fitting a cosine curve to hourly urine aMT6s levels will be determined daily
maximum glucose
highest glucose per day of interest
minimum glucose
lowest glucose per day of interest
insulin usage
number of insulin units used per day (composite of short and long acting formulations)

Full Information

First Posted
May 19, 2020
Last Updated
January 24, 2023
Sponsor
Yale University
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1. Study Identification

Unique Protocol Identification Number
NCT04437264
Brief Title
Intermittent Versus Continuous Enteral Nutrition in Mechanically Ventilated Patients in the Medical Intensive Care Unit
Official Title
Intermittent Versus Continuous Enteral Nutrition in Mechanically Ventilated Patients in the Medical Intensive Care Unit
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 7, 2020 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Evaluate effective delivery of goal nutrition with intermittent as compared with continuous enteral nutrition schedules, as defined by percentage of recommended calories that patient receives per day of interest.
Detailed Description
Eligible patients will be approached and if the patient (or surrogate decision maker) is interested, then consent will be obtained for participation in the study. The patient will then be randomly assigned to receive usual care (continuous feeds) or intervention (intermittent feeds, see details below). Randomization will occur via simple block randomization within the REDCap software. Group assignment will not be revealed to the clinical team until the decision to feed the patient has occurred and the actual feeding order is entered. When the clinical team decides to initiate enteral nutrition, they will place a nutrition consult order for tube feed recommendations. Nutrition consult will place recommendations for both continuous feeding and for intermittent schedule, including enteral nutrition formula and dosing. Prior to feeds being started, the patient's randomization status will be revealed to the clinical team. The covering provider will then place the order for enteral nutrition according to the nutritionist's recommendations for the correct feeding schedule. For patients randomized to continuous feeds, their enteral nutrition will be ordered and delivered as per usual care and standard MICU procedure. Nutritionist will provide recommendations for initiation rate, up titration schedule, and maintenance dosing to be delivered continuously over 24 hours. Under usual care of ICU patients, our clinical nutritionists provide a specified formula, a specified calorie goal, and a suggested titration rate. This is typically 20 mL per hour to start with an increase in rate of 20 mL per hour every 6 to 8 hours until the goal rate is achieved. Typical goal rates are in the range of 60 to 80 mL per hour for 24 hours per day. For patients randomized to the intervention group (intermittent feeds), they will receive their enteral nutrition according to a research protocol schedule. This will involve the total recommended feed volume divided into four equal volume "meals." These will be delivered at a rate of 400 cc/hr at 8:00, 12:00, 16:00, and 20:00. The up-titration schedule will be as follows: first meal will be 100 mL, and the volume of each meal thereafter will be increased by 100mL until patient is at goal volume (typically between 300 and 450 mL). There are no formula or diets that are inappropriate to be administered on an intermittent feed schedule. The intervention will not change formula selection or total calorie goals. It will only change the schedule of feeding. For all patients, regardless of feeding schedule, the Kangaroo E-Pump will be used to deliver enteral nutrition, and the above rate and volume parameters can be programmed in. There will be no change in delivery of enteral free water or medications. This schedule will be determined by nursing and clinical care team, as is the current standard of care. To assure correct ordering of intermittent feeds and the insulin prior to each meal, an EPIC orderset with prepopulated instructions will be developed. If there are no signs of or clinical concerns for intolerance, patients will continue to receive enteral nutrition according to assigned schedule until they are extubated or until enteral nutrition is discontinued.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Enteral Feeding, Nutrition Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The care team and study staff in the ICU will be aware of arm assignment. Study staff abstracting outcome data will be blinded to arm assignement.
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intermittent feed
Arm Type
Experimental
Arm Description
Patients will be assigned to receive intermittent enteral feeding protocol. They will receive four equal volume feeds at 8:00, 12:00, 16:00, and 20:00 hours.
Arm Title
Continuous feeds
Arm Type
Experimental
Arm Description
Patients will be assigned to receive continuous enteral feeding protocol. Typical goal rates are in the range of 60 to 80 mL per hour for 24 hours per day.
Intervention Type
Dietary Supplement
Intervention Name(s)
Intermittent feed participant
Intervention Description
Patients will be assigned to receive intermittent enteral feeding protocol. They will receive four equal volume feeds at 8:00, 12:00, 16:00, and 20:00 hours.
Intervention Type
Dietary Supplement
Intervention Name(s)
Continuous feeds participant
Intervention Description
Patients will be assigned to receive continuous enteral feeding protocol. Typical goal rates are in the range of 60 to 80 mL per hour for 24 hours per day.
Primary Outcome Measure Information:
Title
Recommended calories
Description
percentage of recommended calories that patient receives per day of interest during study period
Time Frame
Intubation day 1 to intubation day 10
Secondary Outcome Measure Information:
Title
Percentage of patients with aspiration
Description
percentage of patients experiencing aspiration
Time Frame
Intubation day 1 to intubation day 10
Title
Percentage of patients experiencing intolerance of feeding
Description
percentage of patients experiencing intolerance of feeding including nausea, vomiting, diarrhea, ileus
Time Frame
Intubation day 1 to intubation day 10
Title
feasibility: proportion complete protocol
Description
percentage of patients assigned to intervention (ie intermittent feeding protocol) that remain on study protocol for study period of interest.
Time Frame
Intubation day 1 to intubation day 10
Title
delirium
Description
number of delirium and coma free days out of 14 following intubation
Time Frame
intubation day 1 until 14 days later
Title
urine 6-sulfatoxymelatonin acrophase
Description
Urine 6-sulfatoxymelatonin acrophase defined as the time of fitted peak 6-sulfatoxymelatonin from fitting a cosine curve to hourly urine aMT6s levels will be determined daily
Time Frame
day 1 to 3 following initiation of feeds
Title
maximum glucose
Description
highest glucose per day of interest
Time Frame
Intubation day 1 to intubation day 10
Title
minimum glucose
Description
lowest glucose per day of interest
Time Frame
Intubation day 1 to intubation day 10
Title
insulin usage
Description
number of insulin units used per day (composite of short and long acting formulations)
Time Frame
Intubation day 1 to intubation day 10

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA MICU Yale New Haven Hospital Age >= 18 years old. Patients mechanically ventilated via endotracheal tube Patients intubated within 72 hours of hospital admission First intubation of current hospitalization First MICU admission of current hospitalization EXCLUSION CRITERIA • Patient has opted out of research participation via institutional patient portal. At significant risk for gastrointestinal intolerance of intermittent bolus feeds: Prior upper gastrointestinal surgery that alters proximal GI anatomy (including but not limited to gastric bypass surgery, gastric banding, complete or partial gastrectomy, Whipple procedure; of note, appendectomy and cholecystectomy are not exclusion criteria. Structural gastrointestinal obstruction (such as tumor). Chronic enteral nutrition (prior to current admission). History of significant esophageal dysmotility (history of GERD is acceptable) or clinically significant GE junction incompetence Unable to have head of bed elevated at least 30 degrees while intubated and being fed (this is standard protocol). Enteral access terminates post-pyloric (ie nasojejunal or jejunostomy tubes are to be excluded) or unable to place gastric tube for access. (The clinical team will determine type of tube placement. As this is particularly selected by intensivists for patients at higher aspiration risk, this tube enteral access exclusion de facto excludes patients at high aspiration risk.) History of small bowel obstruction or ileus on current admission or within last 1 month. History of gastroparesis. Percutaneous gastrostomy tube or tracheostomy. History of ongoing aspiration as determined by a speech medicine specialist or other medical professional or a patent who required adjustment of diet (e.g., thickening of liquids) prior to hospitalization. History of significant esophageal dysmotility (history of GERD is acceptable) or clinically significant GE junction incompetence Other Exclusion Criteria: At risk of refeeding syndrome. Pregnant patients. Patients receiving neuromuscular blockade. Patients with glycemic emergency (HHNK, DKA, severe hypoglycemia resulting in MICU admission) or patients controlling their sugar / insulin dosing via continuous glucose monitoring Post cardiac arrest (on current admission). Received >= 6 hours of enteral nutrition (regardless of volume) at the time of screening and team is able to consent / enroll / initiate intermittent feed within an additional 2 hours. Plan for extubation within 24 hours. Not English-speaking. Patients otherwise excluded by the treating physician. Retrospective exclusion: patients who initially met eligibility criteria, but no nutrition consult (i.e., decision to initiate feeds by clinical providers) placed within 72 hours of intubation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Melissa P Knauert, MD, PhD
Phone
203.785.4163
Email
melissa.knauert@yale.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Taylor A Intihar, BS
Phone
203.785.3207
Email
taylor.intihar@yale.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Melissa P Knauert, MD, PhD
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yale New Haven Hospital, York Street Campus
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06520
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
MICU Director
First Name & Middle Initial & Last Name & Degree
Melissa P Knauert, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
De-identified individual participant data can be made available upon request.

Learn more about this trial

Intermittent Versus Continuous Enteral Nutrition in Mechanically Ventilated Patients in the Medical Intensive Care Unit

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