A Study to Evaluate the Effects of a Butyrate-Polyphenol Formulation on Gut Health and Associated Symptoms

ConditionGut Health
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age25-70
SponsorSupplement Formulators, Inc.

About this trial

The purpose of the study is to evaluate the efficacy of a butyrate/polyphenol formulation on modulation of the gut microbiome and gastrointestinal symptoms using questionnaires in individuals with self-reported gastrointestinal discomfort.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Male or female, age 25-70 years

Body mass index 18.5-34.9 kg/m2

A GSRS-IBS score ≥ 21 (identification as having moderate or severe gastrointestinal symptoms). If the GSRS-IBS score is < 20 (identification of minimal or mild), may be included at the discretion of the PI/Sub-I

Experiencing at least three of the following conditions on a weekly basis (gastrointestinal discomfort, abdominal pain, gas, bloating, diarrhea, or constipation)

Disqualifiers

Currently participating in another clinical research study

Pregnant, planning pregnancy, or breastfeeding

Unable to swallow capsules, tablets, or softgels

Male participants and females of childbearing potential who are unwilling to use an acceptable method of contraception from screening through 30 days after study completion.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Butyrate + Polyphenol Formulation

    Dietary supplement

    Butyrate + Polyphenol Formulation

  • Placebo

    Dietary supplement

    Placebo

Treatment groups

124 Participants
are divided into 2 treatment groups
Group A: Butyrate + Polyphenol FormulationActive comparator 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

The Gastrointestinal Symptom Rating Scale (GSRS)-Irritable Bowel Syndrome (IBS) version

Change in the Gastrointestinal Symptom Rating Scale-IBS from baseline. The responses to the questions range from no discomfort at all to very severe discomfort which would indicate a worse outcome

Time frame
14 days
2

Gut Microbiome Stool Test

Change in the Gut Microbiome (strain level, functional metrics, taxonomy abundance and composition) from baseline

Time frame
14 days

Secondary outcomes

1

Digestion-Associated Quality of Life Questionnaire (DQLQ)

Change in the Digestion-Associated Quality of Life Questionnaire (DQLQ) from baseline. The lower score indicates an improved outcome.

Time frame
14 days
2

Visual Analogue Scale (VAS) of abdominal pain

Change in the Visual Analogue Scale (VAS) of abdominal pain from baseline. The lower the value indicates an improved outcome.

Time frame
14 days
3

Bristol Stool Form Scale (BSFS)

Change in the stool form from baseline. There are 7 various stool types to choose ranging from Type 1 to Type 7. Types 3 or 4 are the preferred types.

Time frame
14 days
4

Gastrointestinal -Global Assessment of Improvement Scale (Gastrointestinal-GAI)

Change in the Gastrointestinal-Global Assessment of Improvement Scale (Gastrointestinal-GAI) from baseline. The responses range from substantially worse to substantially improved would indicate an improved outcome.

Time frame
14 days

Other outcomes

Sponsors and contacts

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