Milk Ingredients and Resistance Against E-coli-induced GastroEnteritis (MIRAGE) (MIRAGE)
Primary Purpose
Bacterial Infection, Diarrhea, Gastroenteritis
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Milk protein
Milk protein rich in phospholipids
Sponsored by
About this trial
This is an interventional prevention trial for Bacterial Infection focused on measuring Bacterial infection, Dairy, Diarrhea, Diet, E.Coli, Gastroenteritis, Milk, Stool consistency
Eligibility Criteria
Inclusion Criteria:
- Signed informed consent
- Age 18-55 yrs
- Availability of internet connection
- Willingness to replace habitual dairy product intake with the supplied low-calcium soy products
- Willingness to abstain from products with high amounts of prebiotic fibers and from products with probiotics starting 1 month prior to study start
- Willingness to give up blood donation from 1 month before the start of the experiment and during the entire experimental period.
Exclusion Criteria:
- Current or previous underlying disease of the GI tract, liver, bile bladder, kidney, thyroid gland (self-reported)
- Allergy to milk products or lactose intolerance (self-reported), since the capsules may contain milk traces from culture media
- Allergy to soy products (self-reported)
- Use of antibiotics, norit, laxatives (up till 6 months prior to inclusion), cholestyramine, acid burn inhibitors or immune suppressive agents (up till 3 months prior to inclusion), and pre- and probiotics (up till 1 month prior to inclusion).
- High titer serum antibodies against ETEC (10 ml blood sample collected at screening)
- ETEC detected in fecal sample (collected at screening)
- Vegetarians
- Vegans
- Heavy alcohol use (>4 consumptions/day or >20/week)
- Drug use
Sites / Locations
- NIZO food research
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Milk protein
Milk protein rich in phospholipids
Arm Description
Milk powder, twice daily at breakfast and dinner.
Milk powder, twice daily at breakfast and dinner.
Outcomes
Primary Outcome Measures
Change of fecal ETEC numbers over time as a marker of intestinal colonization resistance
The change over time in fecal ETEC numbers is compared between treatment and placebo group.
Change of total daily fecal output over time as a marker of infectious diarrhea
The change in the daily fecal output over time is compared between treatment and placebo group.
Secondary Outcome Measures
Daily Bristol Stool Score as a marker for stool consistency
Gastro-Intestinal Symptom Rating Scale (GSRS) for gastro-intestinal complaints
% fecal wet weight as a marker for Diarrhea severity
Stool frequency (number of stools per day)
Days -1 and -2 before ETEC challenge and on days 1-15 after challenge
Specific serum antibody response to CFAII
Full Information
NCT ID
NCT01800396
First Posted
February 21, 2013
Last Updated
August 26, 2015
Sponsor
NIZO Food Research
Collaborators
Arla Foods, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT01800396
Brief Title
Milk Ingredients and Resistance Against E-coli-induced GastroEnteritis (MIRAGE)
Acronym
MIRAGE
Official Title
A Randomized, Placebo-controlled, Double Blind Volunteer Study Into the Effect of Milk Ingredients on Gastroenteritis Caused by an Attenuated E.Coli.
Study Type
Interventional
2. Study Status
Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
May 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NIZO Food Research
Collaborators
Arla Foods, Denmark
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Background: The incidence of gastrointestinal infections is very high. In Western countries at least 30% of the population suffers from at least one food-borne infection per year. Mostly because of the problem of antibiotic resistance, more emphasis is put on prevention of infections. One of the possibilities is to strengthen human resistance to gut infections by consumption of milk ingredients.
Aim: To study whether a milk protein concentrate rich in phospholipids improves the resistance of humans to enterotoxigenic E. coli (ETEC).
Study design: The MIRAGE study is a parallel, double-blind, placebo-controlled 4-weeks intervention with a milk protein concentrate rich in phospholipids in healthy subjects of 18-55 yrs of age. Participants will be randomly assigned to the milk protein concentrate rich in phospholipids or placebo group (n=30 per group). Subjects will be instructed to maintain their usual pattern of physical activity and their habitual food intake, but to standardize their dietary calcium intake. After an adaptation period of 2 weeks, subjects will be orally infected with a live, but attenuated, ETEC vaccine (strain E1392-75-2A; collection NIZO food research; dose will be 1010 CFU). Before and after infection, an online diary will be kept to record all food and drinks consumption (2x2 days) to assess the habitual dietary intake. The diary will also be used for daily recording of bowel habits and frequency and severity of gastrointestinal complaints.
The following biological samples will be collected: 4x10 ml venous blood, a single fecal bolus (for screening) and 7x24 hrs feces. Blood is sampled for immune response analyses and the fecal samples are collected to quantify several infection- and immune system markers and to verify dietary calcium intake. Saliva is sampled three times before and after infection to quantify immune system markers.
Primary outcomes: Fecal ETEC excretion and severity of diarrhea (quantified by fecal output per day).
Secondary outcomes: Serum immune response to ETEC, self-reported stool consistency scores and gastrointestinal complaints, relative fecal wet weight.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bacterial Infection, Diarrhea, Gastroenteritis
Keywords
Bacterial infection, Dairy, Diarrhea, Diet, E.Coli, Gastroenteritis, Milk, Stool consistency
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Milk protein
Arm Type
Placebo Comparator
Arm Description
Milk powder, twice daily at breakfast and dinner.
Arm Title
Milk protein rich in phospholipids
Arm Type
Experimental
Arm Description
Milk powder, twice daily at breakfast and dinner.
Intervention Type
Dietary Supplement
Intervention Name(s)
Milk protein
Intervention Type
Dietary Supplement
Intervention Name(s)
Milk protein rich in phospholipids
Primary Outcome Measure Information:
Title
Change of fecal ETEC numbers over time as a marker of intestinal colonization resistance
Description
The change over time in fecal ETEC numbers is compared between treatment and placebo group.
Time Frame
Days -1 and -2 before ETEC challenge and days 1,2,3,4,7 and 15 after challenge
Title
Change of total daily fecal output over time as a marker of infectious diarrhea
Description
The change in the daily fecal output over time is compared between treatment and placebo group.
Time Frame
Days -1 and -2 before ETEC challenge and on days 1,2,3,4,7 and 15 after challenge.
Secondary Outcome Measure Information:
Title
Daily Bristol Stool Score as a marker for stool consistency
Time Frame
Days -1 and -2 before ETEC challenge and on days 1-15 after challenge.
Title
Gastro-Intestinal Symptom Rating Scale (GSRS) for gastro-intestinal complaints
Time Frame
Days -1 and -2 before ETEC challenge and on days 1-15 after challenge
Title
% fecal wet weight as a marker for Diarrhea severity
Time Frame
Days -1 and -2 before ETEC challenge and days 1-15 after challenge.
Title
Stool frequency (number of stools per day)
Description
Days -1 and -2 before ETEC challenge and on days 1-15 after challenge
Time Frame
Day -1 and -2 and days 0-15
Title
Specific serum antibody response to CFAII
Time Frame
Before ETEC challenge and on day 15 after challenge.
Other Pre-specified Outcome Measures:
Title
Calprotectin in feces
Time Frame
Before ETEC challenge and on day 2 and 3 after challenge.
Title
Total fecal and salivary sIgA
Time Frame
Before ETEC challenge and on day 3 and 4 after challenge.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Signed informed consent
Age 18-55 yrs
Availability of internet connection
Willingness to replace habitual dairy product intake with the supplied low-calcium soy products
Willingness to abstain from products with high amounts of prebiotic fibers and from products with probiotics starting 1 month prior to study start
Willingness to give up blood donation from 1 month before the start of the experiment and during the entire experimental period.
Exclusion Criteria:
Current or previous underlying disease of the GI tract, liver, bile bladder, kidney, thyroid gland (self-reported)
Allergy to milk products or lactose intolerance (self-reported), since the capsules may contain milk traces from culture media
Allergy to soy products (self-reported)
Use of antibiotics, norit, laxatives (up till 6 months prior to inclusion), cholestyramine, acid burn inhibitors or immune suppressive agents (up till 3 months prior to inclusion), and pre- and probiotics (up till 1 month prior to inclusion).
High titer serum antibodies against ETEC (10 ml blood sample collected at screening)
ETEC detected in fecal sample (collected at screening)
Vegetarians
Vegans
Heavy alcohol use (>4 consumptions/day or >20/week)
Drug use
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sandra Ten Bruggencate, PhD
Organizational Affiliation
NIZO food research, The Netherlands
Official's Role
Principal Investigator
Facility Information:
Facility Name
NIZO food research
City
Ede
ZIP/Postal Code
6718ZB
Country
Netherlands
12. IPD Sharing Statement
Citations:
PubMed Identifier
12891550
Citation
Bovee-Oudenhoven IM, Lettink-Wissink ML, Van Doesburg W, Witteman BJ, Van Der Meer R. Diarrhea caused by enterotoxigenic Escherichia coli infection of humans is inhibited by dietary calcium. Gastroenterology. 2003 Aug;125(2):469-76. doi: 10.1016/s0016-5085(03)00884-9.
Results Reference
background
PubMed Identifier
26701793
Citation
Ten Bruggencate SJ, Frederiksen PD, Pedersen SM, Floris-Vollenbroek EG, Lucas-van de Bos E, van Hoffen E, Wejse PL. Dietary Milk-Fat-Globule Membrane Affects Resistance to Diarrheagenic Escherichia coli in Healthy Adults in a Randomized, Placebo-Controlled, Double-Blind Study. J Nutr. 2016 Feb;146(2):249-55. doi: 10.3945/jn.115.214098. Epub 2015 Dec 23.
Results Reference
derived
Links:
URL
http://www.nizo.com
Description
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Milk Ingredients and Resistance Against E-coli-induced GastroEnteritis (MIRAGE)
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