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Late Evening and Early Morning Protein Supplement to Reduce Readmissions for Hepatic Encephalopathy

Primary Purpose

Hepatic Encephalopathy

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ensure Enlive
Standard Of Care
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatic Encephalopathy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • > 18 years of age
  • cirrhosis diagnosed by clinical history and liver biopsy and/or clinical, biochemical and imaging evidence of cirrhosis
  • at least 1 hospitalization for documented HE within the last 12 months.
  • abdominal CT scan anytime in the past

Exclusion Criteria:

  • Patients with MELD score > 35
  • end stage organ failure (major dysfunction requiring organ support)
  • kidney injury defined by a creatinine > 2 mg/dl or rise in creatinine by 0.5 gm/dl from baseline that is unresponsive to withholding diuretics and intravenous albumin administration (1 gm/kg up to 100 gm/day)
  • active malignancy
  • uncontrolled diabetes mellitus with A1c>9.5 (to avoid altered muscle protein metabolism
  • medications (anabolic steroids, corticosteroids) that affect skeletal muscle mass
  • recent gastrointestinal surgery within past 12 months
  • ongoing infection (positive blood or other body fluid cultures)
  • active gastrointestinal bleeding.

Sites / Locations

  • Cleveland Clinic FoundationRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Ensure Enlive

Standard of Care

Arm Description

Outcomes

Primary Outcome Measures

Determine if decreasing nocturnal fasting by protein supplements will change readmission rates.
Change in number of readmissions

Secondary Outcome Measures

Full Information

First Posted
September 11, 2019
Last Updated
June 26, 2023
Sponsor
The Cleveland Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT04096014
Brief Title
Late Evening and Early Morning Protein Supplement to Reduce Readmissions for Hepatic Encephalopathy
Official Title
Late Evening and Early Morning Protein Supplement to Reduce Readmissions for Hepatic Encephalopathy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 16, 2019 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
October 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Cleveland Clinic

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
Readmission rates for patients with hepatic encephalopathy due to end stage liver disease are high. Hyperammonemia contributes significantly to encephalopathy and occurs because of impaired hepatic ureagenesis and increased skeletal muscle proteolysis. We propose a randomized, 6-month nutritional intervention in cirrhotic patients who have had at least 1 admission for hepatic encephalopathy within the last 6 months. We hypothesize that a combination of late evening and early morning protein supplement (Ensure Enlive) will decrease recurrent hepatic encephalopathy and consequent readmission rates by lowering skeletal muscle proteolysis and improved lean body mass.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatic Encephalopathy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ensure Enlive
Arm Type
Active Comparator
Arm Title
Standard of Care
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Ensure Enlive
Intervention Description
The subjects in the intervention group will receive two Ensure Enlive supplements per day for 180 days.
Intervention Type
Other
Intervention Name(s)
Standard Of Care
Intervention Description
The subjects in the Standard of care group will continue to receive the standard clinical therapy.
Primary Outcome Measure Information:
Title
Determine if decreasing nocturnal fasting by protein supplements will change readmission rates.
Description
Change in number of readmissions
Time Frame
Day 0 & Day 180

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: > 18 years of age cirrhosis diagnosed by clinical history and liver biopsy and/or clinical, biochemical and imaging evidence of cirrhosis at least 1 hospitalization for documented HE within the last 12 months. abdominal CT scan anytime in the past Exclusion Criteria: Patients with MELD score > 35 end stage organ failure (major dysfunction requiring organ support) kidney injury defined by a creatinine > 2 mg/dl or rise in creatinine by 0.5 gm/dl from baseline that is unresponsive to withholding diuretics and intravenous albumin administration (1 gm/kg up to 100 gm/day) active malignancy uncontrolled diabetes mellitus with A1c>9.5 (to avoid altered muscle protein metabolism medications (anabolic steroids, corticosteroids) that affect skeletal muscle mass recent gastrointestinal surgery within past 12 months ongoing infection (positive blood or other body fluid cultures) active gastrointestinal bleeding.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Annette C Bellar
Phone
2166365247
Ext
2166365247
Email
bellara@ccf.org
Facility Information:
Facility Name
Cleveland Clinic Foundation
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Annette Bellar, BS
Phone
216-445-6268
Email
bellara@ccf.org
First Name & Middle Initial & Last Name & Degree
Revathi Penumatsa
Email
penumar@ccf.org
First Name & Middle Initial & Last Name & Degree
Srinivasan Dasarathy, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Late Evening and Early Morning Protein Supplement to Reduce Readmissions for Hepatic Encephalopathy

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