A Clinical Trial to Evaluate the Effects of a Supplement on Gut Health

What this study involves

The registry says this study is recruiting. Individual locations may have different availability.

Study type

Interventional

Phase

Not applicable

Age range

18 years - 60 years

Sex eligible

All sexes

Healthy volunteers

Not accepted

Participants

40 Estimated

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

This study will evaluate the effects of the Peachbiotic supplement on gut health in adults experiencing gastrointestinal symptoms. The trial is a single-arm, open-label, virtual study in which all 40 enrolled participants will use the test product daily for 12 weeks.

Participants will take one capsule of the product once daily in the morning with food and will complete self-reported questionnaires at Baseline, Week 4, Week 8, and Week 12 to assess changes in gut health outcomes including bloating, digestive comfort, regularity of bowel movements, gasiness, and general well-being.

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

Inclusion Criteria:

• Be male or female
• Be aged 18-60
• Anyone who has been experiencing issues regarding at least two of the following for the past month: stomach discomfort, constipation, diarrhea, heartburn, bloating, gas, or abdominal pain
• If taking any other supplements or herbal remedies that target gut or digestive health, has been doing so consistently for at least three months and is willing to maintain this for the duration of the study
• Anyone willing to avoid introducing any other new supplements, medications, or herbal remedies for the duration of this trial
• Anyone willing to maintain their current diet, sleep pattern, and activity levels for the duration of the trial
• Anyone in good general health
• Resides in the United States

Exclusion Criteria:

• Anyone with a known history of severe digestive disorders like acid reflux, Irritable Bowel Syndrome (IBS), Irritable Bowel Disease (IBD), Crohn's disease, or gastrointestinal tract surgeries
• Anyone with any known allergies or hypersensitivities to any supplement product ingredients
• Anyone with a pineapple allergy
• Anyone with any chronic health conditions that could impact participation in this study, such as cancer, mental health disorders, history of serious illness in the last three months, history of substance abuse, or planned surgery during the study period
• Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period)
• Anyone currently taking prescription anticoagulants ('blood thinners') or with a history of a bleeding disorder
• Anyone unwilling to follow the study protocol
• Currently partaking in another research study or will be partaking in any other research study at any point during this study's duration

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment

Not applicable

Masking

No masking

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Secondary measures

Research locations (1)

The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.

1 locations

Study team and timeline

Lead sponsor

Peach Perfect

Study start

Feb 1, 2026 Actual

Primary completion

Nov 1, 2026 Estimated

Study completion

Nov 1, 2026 Estimated

First posted

Nov 10, 2026 Actual

Last updated

Nov 10, 2026 Actual

Official study contacts