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OpenTrials
Completed

NCT Number: NCT04065503

Probiotic Detection and Persistence Study

The aims of this study are to determine how long it takes for the strains of a probiotic formulation to be detected in feces after the start of an intervention, how long they persist after the end of the intervention, and the associations between detection and persistence with total gut transit time.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Food Science and Human Nutrition Department

Gainesville, Florida, 32611, United States

About this study

This is a 10-week interventional, open-label pilot study designed to evaluate the detection and persistence of L. helveticus R-0052, L. casei NI319, B. breve NI337, and B. longum R-0175 strains in feces of healthy adults following the start and the end of IP intervention, respectively. This study will have an initial baseline period (4 weeks), a probiotic intervention (2 weeks) and a washout period (4 weeks). Participants will complete daily questionnaires regarding stool frequency, time of stool collections, and IP intake. A weekly Gastrointestinal Symptom Rating Scale (GSRS) questionnaire will be administered. Transit time will be assessed using radiopaque markers.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy adults ≥ 18 to < 55 years of age.
  • Habitually produces at least one bowel movement per day.
  • Willingness to maintain their usual diet and exercise patterns throughout the study.
  • Able to provide written informed consent in English.
  • Willing to provide stools and complete questionnaires, records, and diaries associated with the study and to complete all study visits.
  • Willingness to discontinue consumption of probiotics and fermented products (e.g. yogurts, kombucha, fermented pickles and other fermented foods with live, active cultures) and probiotic supplements.

Exclusion criteria

  • Elite athletes or long-distance runners.
  • Concurrent consumption of fermented foods or probiotics. However, individuals will be eligible for participation after a four (4) week wash-out period.
  • Known to be pregnant (self-disclosure) or breastfeeding or planning on becoming pregnant in the next 2 months.
  • Use of antibiotic drugs (e.g., neomycin, rifaximin) within 1 month of the screening visit. The screened participant would be eligible to participate four (4) weeks after completing their course of antibiotics (washout period).
  • Use of other investigational products within 3 months of the screening visit.
  • Previously or are currently being treated for any previously or currently being treated for any intestinal disease or condition such as IBS, Crohn's disease, ulcerative colitis, celiac disease, or gastrointestinal cancer.
  • Immune disorders or with possible immune deficient status (e.g. due to surgery).
  • Milk or soy allergy.

Treatment and study plan

Probiotic Strains

Biological

A commercial product containing L. helveticus R0052, L. casei HA-108, B. breve HA-129, and B. longum R0175 and S. thermophilus HA-110 be given to healthy adults across a 10-week open label pilot study.

Primary outcomes

  1. Change in time to detection of probiotic strains

    Time frame: Day 1; Day 2; Day 3, Day 4, Day 7, Day 10

    using strain-specific qPCR assays.

  2. Change in time to non-detection (persistence) of probiotic strains

    Time frame: Day 14, Day 15, Day 16, Day 17, Day 18, Day 21, Day 24, Day 28, Day 35, Day 42

    using strain-specific qPCR assays.

Secondary outcomes

  1. Whole gut transit time

    Time frame: Day 1, Day 2, Day 3, Day 4

    Whole gut transit time measured by radiopaque marker recovery in intervention stools

Sponsors and collaborators

Lead sponsor

University of Florida

Other

Collaborators

  • Lallemand Health Solutions, Inc.

Registry information

Official study title

Detection and Persistence of a Product Containing L. Helveticus R-0052, L. Casei HA-108, B. Breve HA-129, B. Longum R-0175 and S. Thermophilus HA-110 in Healthy Adults: an Open-label Pilot Study.

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Aug 22, 2019
Registry last updated
Jan 19, 2021

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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