Gut health follow-along with Peachbiotic in adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This 12-week, open-label study gives 40 adults daily Peachbiotic capsules to see if gut symptoms improve. Participants complete questionnaires at baseline, 4, 8, and 12 weeks, reporting bloating, digestive comfort, bowel regularity, gas, and general well-being. The study is virtual, with data collected remotely and no control group. It focuses on adults aged 18–60 living in the United States who have at least two digestive symptoms. Probiotics and Fibruline Inulin Powder are used as the intervention, and participants should avoid starting new gut-related remedies during the trial.

Why it matters

Who can join: the full rules

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

Where it's running

• Citruslabs
  Las Vegas, Nevada, United States Recruiting

Study contacts

• Study coordinator: Patrick Renner
• Email: hello@citruslabs.com
• Phone: 520-298-7494

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.