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

Part of paid clinical trials in Fort Lauderdale, Florida.

Sponsor
Supplement Formulators, Inc.
Study ID
NCT07371975
Status
Recruiting
Apply to this trial

Conditions

  • Gut Health

Eligibility Criteria

Sex
ALL
Age
25 Years - 70 Years
Healthy Volunteers
Accepted

Interventions

  • Butyrate + Polyphenol Formulation — DIETARY_SUPPLEMENT
    Butyrate + Polyphenol Formulation
  • Placebo — DIETARY_SUPPLEMENT
    Placebo

Study Details

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.

Key Dates

Start date
Oct 16, 2025
Status verified
Jan 2026
Primary completion
Apr 26, 2026
Completion
Jul 30, 2026

Study Design

Enrollment
124 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Butyrate + Polyphenol Formulation
    Butyrate + Polyphenol Formulation
  • Placebo Comparator: Placebo

Primary Outcome Measure

The Gastrointestinal Symptom Rating Scale (GSRS)-Irritable Bowel Syndrome (IBS) version [ Time Frame: 14 days ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Life Extension Clinical Research, Inc.Fort LauderdaleFlorida33304
Steven Hirsh
[email protected]
954-202-7679
Barbara Martinez
[email protected]
9542842709
Andrew Swick, PhD (PRINCIPAL_INVESTIGATOR)

Find similar trials in Fort Lauderdale, FL

By research site
Life Extension Clinical Research, Inc.· Fort Lauderdale, FL

Related Studies