Recruiting

Peachbiotic

Sponsor:

Peach Perfect

Code:

NCT07927907

Conditions

Gut Health

Bloating

Digestive Discomfort

Constipation

Diarrhea

Eligibility Criteria

Sex: All

Age: 18 - 60

Healthy Volunteers: Not accepted

Interventions

Intervention Probiotics, Fibruline® Inulin Powder

Study Details

Brief summary:

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.

Conditions

Gut Health

Bloating

Digestive Discomfort

Constipation

Diarrhea

Study ID

NCT07927907

Start date

Feb 1, 2026

Status verified date

Nov, 2026

Completion date

Nov 1, 2026

Anticipated

Primary completion date

Nov 1, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 60

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

40 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Probiotics, Fibruline® Inulin Powder

Interventions

Intervention Probiotics, Fibruline® Inulin Powder

All participants will use the test product. Participants will answer questionnaires at Baseline, Week 4, Week 8, and Week 12.

Primary outcome measure

  • Change in Gut Health (GSRS) [ Time Frame: Baseline, Week 4, Week 8, and Week 12 ]
  • Change in Gut Health (Bristol Stool Scale) [ Time Frame: Baseline, Week 4, Week 8, and Week 12 ]

Central Contacts and Locations

Central contacts

Locations

Citruslabs

Recruiting

Las Vegas, Nevada, United States, 89101

More Information

Sponsor

Peach Perfect

Last update posted

Nov 10, 2026

Last verified

Nov, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-11-11. This information was provided to ClinicalTrials.gov by Peach Perfect on 2026-11-10. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.