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OpenTrials
Completed

NCT Number: NCT07618026

Establishing Effects of Bacillus Clausii Probiotic Consumption on Gastrointestinal Health and Inflammation

The study is a randomized, double-blind, crossover, placebo-controlled clinical intervention trial to test the effects of a commercial Bacillus (Shouchella) clausii probiotic compared to a placebo on gastrointestinal symptoms.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Food and Nutrition Clinical Research Laboratory

Fort Collins, Colorado, 80523, United States

About this study

Prospective participants are pre-qualified by email screening and attended an in-person study visit at Colorado State University's Food and Nutrition Clinical Research Laboratory (FNCRL) in the Department of Food Science and Human Nutrition. During the initial visit, participants signed the Consent Form after the nature of the procedure had been fully explained to them. Their eligibility is confirmed by taking anthropometric measurements of height (cm) and weight (kg) to calculate BMI and by completing a written medical health questionnaire to determine medical history and current medication use. Eligible participants are then assigned sequentially to a study code (MS01, MS02, etc.), and codes were pre-assigned to intervention sequences using a random number generator in Microsoft Excel. For the initial clinic visit (and subsequent visits), participants are fasted for at least 8 hours and asked to abstain from alcohol use for at least 12 hours prior to clinic visits. They were also instructed to refrain from taking any non-prescription medications for 24 hours or dietary supplements for 12 hours before their visits. At the initial visit, a venous blood sample was collected, and participants filled out several assessment forms/questionnaires: GI Health Appraisal Questionnaire, GI Symptom Rating Scale (GSRS), GI Quality of Life Questionnaire (IBS-QOL Questionnaire) 7-day Physical Activity Recall, Positive and Negative Affect Schedule, and Perceived Stress Scale.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Age 18-75
  • BMI 18-34.9
  • self report as healthy
  • consistent Mild to Moderate gastrointestinal distress (determined by a functional GI screen)

Exclusion criteria

  • <18 or >75
  • BMI <18 or >34.9
  • antibiotics within two months
  • probiotic/prebiotic supplements within two weeks prior to the screening process
  • pregnant or breastfeeding
  • taking medications that influence study endpoints of the study (i.e., statins, metformin, nonsteroidal anti-inflammatory drugs, and monoamine oxidase inhibitors)
  • a current diagnosis of cancer, liver or kidney disease, metabolic disorders, and GI diseases (Celiac disease, inflammatory bowel disease, and peptic ulcer disease)

Treatment and study plan

Bacillus (Shouchella) clausii CSI08

Dietary Supplement

Gram-positive, spore-forming microorganism

Other names: Munispore

Placebo

Other

Inert filler material delivered in a capsule identical to the probiotic intervention

Primary outcomes

  1. Adverse Event Rate

    Time frame: 12 weeks

    For each arm adverse event forms were tracked and the total rate of adverse events was calculated

  2. Gastrointestinal symptom rating score

    Time frame: 12 weeks

    Gastrointestinal symptoms were assessed using the gastrointestinal symptom rating score, at the beginning and end of each intervention period. The GSRS is a 15-item scale where each item can be scored 1-7 according to symptom severity. A minimum score is 15 and the maximum score is 110. The higher score indicates more severe symptoms.

Secondary outcomes

  1. Gut microbiota composition

    Time frame: 12 weeks

    The gut microbiota composition was assessed by 16s rRNA at the beginning and end of each intervention period.

  2. Systemic Inflammation

    Time frame: 12 weeks

    PBMCs were collected at the beginning and end of each intervention period and then cultured and stimulated with bacterial LPS. Collected supernatants were assessed using a multiplex ELISA for T-cell activity.

  3. Regularity of Bowel Movements

    Time frame: 13 weeks

    A Bristol stool scale was used to record daily bowel movements throughout the study to determine changes in bowel movement regularity.

Other outcomes

  1. Blood Lipids

    Time frame: 12 weeks

    Blood lipids were assessed using collected whole blood samples at the beginning and end of each intervention period using a Piccolo Xpress Blood Lipid Panel.

  2. Liver Toxicity

    Time frame: 12 weeks

    A comprehensive metabolic panel will be performed on whole blood collected at the beginning and end of each intervention period using a Piccolo Xpress Comprehensive Metabolic Panel. This includes multiple markers, that when considered together, can provide an indication of liver toxicity. Specifically, out-of-range values for alanine amino transferase (ALT), asparagine amino transferase (AST), alkaline phosphatase (AST), bilirubin, albumin, and total protein can collectively be interpreted to look for indication of hepatocellular or cholestatic injury.

Sponsors and collaborators

Lead sponsor

Colorado State University

Other

Collaborators

  • ADM Deerland

Registry information

Official study title

MUNISPORE: Establishing Effects of Bacillus Clausii Probiotic Consumption on Gastrointestinal Health and Inflammation

Acronym: MUNISPORE

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jun 1, 2026
Registry last updated
Jun 1, 2026

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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