The Effect of Probiotics on E. Coli-induced Gastroenteritis

Diarrhea Clinical Trial

— PROTETEC  

Official title:

A Randomized, Placebo-controlled, Double Blind Volunteer Study Into the Effect of Probiotics on Gastroenteritis Caused by an Attenuated E. Coli.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01709266
• Other study ID #: NL40301.081.12
• Status: Completed
• Phase: N/A
• First received: October 11, 2012
• Last updated: August 26, 2015
• Start date: August 2012
• Est. completion date: November 2012

Study information

• Verified date: August 2015
• Source: NIZO Food Research
• Contact: n/a
• Is FDA regulated: No
• Health authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
• Study type: Interventional

Clinical Trial 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 probiotics. A specific blend of probiotic lactic acid bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bifidobacterium longum Rosell-175) and a probiotic yeast (Saccharomyces boulardii), improved stool consistency and shortened the duration of diarrhea in a rat model of E.coli-induced diarrhea. These probiotics showed synergistic effects compared with administration of solely S. boulardii or a mixture of L. helveticus Rosell-52, L. rhamnosus Rosell-11, B. longum Rosell-175. Consumption of S. boulardii and a combination of L. helveticus Rosell-52, L. rhamnosus Rosell-11 reduced diarrhea in humans.

Aim:

To study whether probiotics improves the resistance of humans to enterotoxigenic E. coli (ETEC).

Study design:

The PROTETEC study is a parallel, double-blind, placebo-controlled 4-weeks intervention with probiotics in healthy volunteers. In this study, the effect of probiotic intervention vs placebo on several infection markers in response to an ETEC challenge is investigated. Participants will be randomly assigned to the probiotic 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 10E10 CFU). Before and after infection, a diary will be kept to record all food and drinks consumption (2x2 days) to assess the habitual dietary intake, as well as 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, to determine probiotic excretion, and to verify dietary calcium intake.

Study population:

Healthy males of 20-55 yrs of age.

Interventions:

Probiotics (capsules containing freeze-dried powder, probiotic dose per capsule 5x10E9 CFU; twice daily) or placebo (capsules with carrier material powder of identical appearance)

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.

Tertiary outcomes:

sIgA and calprotectin in feces, probiotic persistence and levels of opportunistic pathogens in the endogenous microbiota.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: November 2012
• Est. primary completion date: November 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 20 Years to 55 Years

Eligibility

Inclusion Criteria:

• Signed informed consent

• Male

• Age 20-55 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 (except for the supplied one) starting 1 month prior to study start

• Willingness to give 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)

• Vegetarians

• Vegans

• Heavy alcohol use (>4 consumptions/day or >20/week)

• Drug use

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Bacterial Infection
• Bacterial Infections
• Diarrhea
• Gastroenteritis

Intervention

Dietary Supplement:
• Probiotics

• Placebo

Locations

Country	Name	City	State
Netherlands	NIZO Food Research	Ede	Utrecht

Sponsors (2)

Lead Sponsor	Collaborator
NIZO Food Research	Lallemand Health Solutions

Country where clinical trial is conducted

Netherlands, 

References & Publications (1)

Ten Bruggencate SJ, Girard SA, Floris-Vollenbroek EG, Bhardwaj R, Tompkins TA. The effect of a multi-strain probiotic on the resistance toward Escherichia coli challenge in a randomized, placebo-controlled, double-blind intervention study. Eur J Clin Nutr — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Opportunistic pathogens in feces	Measurement of tertiary study outcomes will depend on the results of the primary and secondary study outcomes.	1-2 days before ETEC infection, and on selected time points after infection (day 1, 2, 3, 4, 7 or 15, depending on results of primary and secondary outcomes).	No
Other	Calprotectin in feces	Measurement of tertiary study outcomes will depend on the results of the primary and secondary study outcomes.	1-2 days before ETEC infection, and on selected time points after infection (day 1, 2, 3, 4, 7 or 15, depending on results of primary and secondary outcomes).	No
Other	Total faecal sIgA	Measurement of tertiary study outcomes will depend on the results of the primary and secondary study outcomes.	1-2 days before ETEC infection, and on seleceted time points after infection (day 1, 2, 3, 4, 7 or 15, depending on results of primary and secondary outcomes).	No
Primary	Fecal ETEC excretion curve over time as marker of the colonization resistance	The curve of fecal ETEC excretion over time is compared between verum and placebo group.	Fecal ETEC excretion measured 1-2 days before ETEC infection, and on day 1, 2, 3, 4, 7 and 15 after infection.	No
Primary	Total daily fecal output curve over time as marker of diarrhea	The curve of daily fecal output over time is compared between verum and placebo group.	Daily fecal output is measured 1-2 days before ETEC infection (baseline), and on day 1, 2, 3, 4, 7 and 15 after infection.	No
Secondary	Bowel habits		Scored daily in a diary during 4 weeks, starting at the day of dietary intervention until 2 weeks after ETEC infection.	No
Secondary	Frequency and severity of gastrointestinal symptoms		Scored daily by VAS scores in a diary during 4 weeks, starting at the day of dietary intervention until 2 weeks after ETEC infection.	No
Secondary	Diarrhea severity	Measured by fecal dry weight excretion and % fecal dry weight.	1-2 days before ETEC infection, and on day 1, 2, 3, 4, 7 and 15 after infection.	No
Secondary	Specific serum antibody response to CFA-II		Before and at day 3 and 15 after ETEC infection.	No