NIZO food research
Ede, 6718 ZB, Netherlands
NCT Number: NCT01225042
Background:
The incidence of gastrointestinal infections is very high. In European countries 10-25% of the population suffers from at least one foodborne infection per year. Probiotics may strengthen human resistance to gut infections as they may beneficially modulate the intestinal microbiota composition and activity, and the immune function upon intestinal infection.
Aim:
To study whether probiotics improve the resistance of humans to enterotoxigenic E. coli (ETEC).
Study design:
The PRETEC study is a parallel, double-blind, placebo-controled 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=21 per group). Subjects will be instructed to maintain 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 10E10 CFU). This ETEC strain induces mild and short-lived infectious diarrhea symptoms. Before and after infection, a diary will be kept to write down 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. Blood is sampled for immune response analyses and multiple faecal 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 (freeze-dried powder, dose 10E9 CFU twice daily) or placebo (carrier material powder of identical appearance).
Primary outcomes:
Total fecal ETEC excretion per day and severity of diarrhea (quantified by faecal output per day).
Secondary outcomes:
Serum immune response to ETEC, self-reported stool consistency scores and gastrointestinal complaints, relative faecal wet weight, sIgA and calprotectin in faeces, probiotic persistence and levels of opportunistic pathogens in the endogenous microbiota.
Looking for future studies?
Notify Me20 year–55 year
Male
Interventional
Not applicable
Ede, 6718 ZB, Netherlands
The timeframes for analysis of the primary and secondary outcomes is mentioned below in the Outcome Measures section.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Freeze-dried powder, dose 10E9 CFU twice daily for 4 weeks
placebo consisting of carrier material powder of identical appearance
Time frame: 1-2 days before ETEC infection and on days 1, 2, 3, 5 and 15 after ETEC infection
Time frame: 1-2 days before ETEC infection and on days 1, 2, 3, 5, 15 after ETEC infection
Time frame: Scored daily in a diary
Time frame: Scored daily by VAS scales in a diary
Time frame: 1-2 days before ETEC infection and on days 1, 2, 3, 5, and 15 after ETEC infection
Determined as % faecal wet weight
Time frame: At a single day just before ETEC infection and at a single time point in the first week after ETEC infection
Time frame: 1-2 days before ETEC infection and on days 1, 2, 3, 5, and 15 after ETEC infection
Time frame: At screening (baseline) and at days 9 and 15 after ETEC infection
Time frame: 1-2 days before ETEC infection and on days 1, 2, 3, 5, and 15 after ETEC infection
NIZO Food Research
Other
Acronym: PRETEC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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