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Ganglioside and IBD

Primary Purpose

Inflammatory Bowel Diseases

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Buttermilk Powder
Anhydrous Milk Fat
Sponsored by
Children's Hospital of Orange County
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammatory Bowel Diseases

Eligibility Criteria

9 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Participants age 9-21 years
  2. Mild-moderate IBD defined by ImproveCareNow (ICN) Physician Global Assessment (PGA); OR severe IBD defined by ICN PGA if stable for at least 120 days
  3. Ileal, ileocolonic, colonic location of disease

Exclusion Criteria:

  1. Pregnancy
  2. Previous bowel resection
  3. Non-ileocolonic location of disease
  4. Inadequate liver or renal function
  5. On prescription medication for active infectious disease
  6. Drug/alcohol abuse
  7. Other serious medical conditions

Sites / Locations

  • Children's Hospital of Orange CountyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Treatment

Placebo

Arm Description

5 grams of buttermilk powder daily for 10 weeks, oral.

5 grams of milk powder (10% buttermilk powder, 90% anhydrous milk fat) daily for 10 weeks, oral.

Outcomes

Primary Outcome Measures

Disease activity index
Pediatric 1) Crohn Disease or 2) Ulcerative Colitis disease activity index
Disease activity index
Pediatric 1) Crohn Disease or 2) Ulcerative Colitis disease activity index

Secondary Outcome Measures

ImproveCareNow Physician Global Assessment
A disease activity index
ImproveCareNow Physician Global Assessment
A disease activity index
IMPACT-III questionnaire
quality of life scales (0 = lowest, 100 = highest): well-being, emotional functioning, social functioning, body image
IMPACT-III questionnaire
quality of life scales (0 = lowest, 100 = highest): well-being, emotional functioning, social functioning, body image
Intestinal integrity
Intestinal permeability (lactulose/mannitol) challenge
Intestinal integrity
Intestinal permeability (lactulose/mannitol) challenge
Calprotectin
Stool test
Calprotectin
Stool test
C-reactive protein
Blood test
C-reactive protein
Blood test

Full Information

First Posted
February 23, 2021
Last Updated
July 25, 2022
Sponsor
Children's Hospital of Orange County
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1. Study Identification

Unique Protocol Identification Number
NCT04782544
Brief Title
Ganglioside and IBD
Official Title
Assessing Whether Buttermilk Powder Improves Disease Activity in Pediatric IBD
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 28, 2021 (Actual)
Primary Completion Date
June 15, 2023 (Anticipated)
Study Completion Date
September 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital of Orange County

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
Context. Inflammatory bowel disease (IBD) is a chronic and debilitating disorder. Novel treatment strategies aimed to resolve intestinal inflammation and induce disease remission are necessary. Dietary gangliosides are safe for consumption, bioavailable, and have shown clinical benefit in patients with inflammatory intestinal disease. Objectives. The primary objective is this study is to determine the efficacy of dietary ganglioside in improving disease activity indices in pediatric patients with IBD. Secondary objectives include demonstrating the effectiveness of dietary ganglioside for improving quality of life, improving intestinal integrity, and reducing inflammation. Study Design. Intervention: controlled trial (pilot). Participants. Inclusion criteria: aged 9-21 years, diagnosis of ulcerative colitis (UC) or ileal or colonic Crohn Disease (CD), active disease. Exclusion criteria: pregnancy, inadequate liver or renal function, active infectious disease, previous bowel resection, disease remission, drug/alcohol abuse, other serious medical conditions, indeterminate colitis. Study Intervention. Patients with IBD (n=48) will be allocated to consume ganglioside treatment or placebo daily for 10 weeks. Treatment group will consume five grams of buttermilk powder daily or anhydrous milk fat. Outcome Measures. The primary outcome is the disease activity index: pediatric Crohn's Disease Activity Index (pCDAI) or pediatric Ulcerative Colitis Activity Index (pUCAI). Secondary outcomes include: quality of life (IMPACT-III questionnaire), intestinal permeability (lactulose/mannitol urinary assay), C-reactive protein (CRP; blood exam), calprotectin (fecal exam). Expected Outcomes. Relative to the placebo group, the treatment group will have improved disease activity indices, quality of life, and intestinal integrity over the 10-week study period. The treatment group will also show reduction in inflammation and calprotectin relative to the placebo group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Non-Randomized
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Active Comparator
Arm Description
5 grams of buttermilk powder daily for 10 weeks, oral.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
5 grams of milk powder (10% buttermilk powder, 90% anhydrous milk fat) daily for 10 weeks, oral.
Intervention Type
Other
Intervention Name(s)
Buttermilk Powder
Intervention Description
Treatment with 5.0 g of buttermilk powder daily for 10 weeks.
Intervention Type
Other
Intervention Name(s)
Anhydrous Milk Fat
Intervention Description
Treatment with 5.0 g of milk powder (90% anhydrous milk fat, 10% buttermilk powder) daily for 10 weeks.
Primary Outcome Measure Information:
Title
Disease activity index
Description
Pediatric 1) Crohn Disease or 2) Ulcerative Colitis disease activity index
Time Frame
Day 0
Title
Disease activity index
Description
Pediatric 1) Crohn Disease or 2) Ulcerative Colitis disease activity index
Time Frame
Day 70
Secondary Outcome Measure Information:
Title
ImproveCareNow Physician Global Assessment
Description
A disease activity index
Time Frame
Day 0
Title
ImproveCareNow Physician Global Assessment
Description
A disease activity index
Time Frame
Day 70
Title
IMPACT-III questionnaire
Description
quality of life scales (0 = lowest, 100 = highest): well-being, emotional functioning, social functioning, body image
Time Frame
Day 0
Title
IMPACT-III questionnaire
Description
quality of life scales (0 = lowest, 100 = highest): well-being, emotional functioning, social functioning, body image
Time Frame
Day 70
Title
Intestinal integrity
Description
Intestinal permeability (lactulose/mannitol) challenge
Time Frame
Day 0
Title
Intestinal integrity
Description
Intestinal permeability (lactulose/mannitol) challenge
Time Frame
Day 70
Title
Calprotectin
Description
Stool test
Time Frame
Day 0
Title
Calprotectin
Description
Stool test
Time Frame
Day 70
Title
C-reactive protein
Description
Blood test
Time Frame
Day 0
Title
C-reactive protein
Description
Blood test
Time Frame
Day 70
Other Pre-specified Outcome Measures:
Title
Hemoglobin, study start
Description
g/L, from metabolic panel
Time Frame
Day 0
Title
Hemoglobin, study end
Description
g/L, from metabolic panel
Time Frame
Day 70
Title
Platelets, study start
Description
#, from metabolic panel
Time Frame
Day 0
Title
Platelets, study end
Description
#, from metabolic panel
Time Frame
Day 70
Title
White blood cells, study start
Description
#, from metabolic panel
Time Frame
Day 0
Title
White blood cells, study end
Description
#, from metabolic panel
Time Frame
Day 70
Title
Albumin, study start
Description
g/L, from metabolic panel
Time Frame
Day 0
Title
Albumin, study end
Description
g/L, from metabolic panel
Time Frame
Day 70
Title
Hematocrit, study start
Description
proportion, from metabolic panel
Time Frame
Day 0
Title
Hematocrit, study end
Description
proportion, from metabolic panel
Time Frame
Day 70

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants age 9-21 years Mild-moderate IBD defined by ImproveCareNow (ICN) Physician Global Assessment (PGA); OR severe IBD defined by ICN PGA if stable for at least 120 days Ileal, ileocolonic, colonic location of disease Exclusion Criteria: Pregnancy Previous bowel resection Non-ileocolonic location of disease Inadequate liver or renal function On prescription medication for active infectious disease Drug/alcohol abuse Other serious medical conditions
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Megan A Bailey
Phone
714-509-8869
Email
mebailey@choc.org
Facility Information:
Facility Name
Children's Hospital of Orange County
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elisa Ornelas
Phone
714-509-8765
Email
elisa.ornelas@choc.org

12. IPD Sharing Statement

Plan to Share IPD
No

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Ganglioside and IBD

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