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Study to Evaluate the Efficacy of Poppi Apple Cider Vinegar Prebiotic Soda to Improve Gut Health In Participants

D

Drink Poppi

Status

Completed

Conditions

IBS - Irritable Bowel Syndrome

Treatments

Dietary Supplement: Drink Poppi Soda

Study type

Interventional

Funder types

Industry

Identifiers

NCT05418439
20229 Poppi

Details and patient eligibility

About

This exploratory observational trial provides the opportunity to gather information on the effect of daily consumption of Poppi Apple Cider Vinegar Prebiotic Soda on gut health and digestion.

Full description

Individuals aged 18+ with a BMI under 30 and self-reported regular issues with IBS and/or poor digestion symptoms, including bloating, gassiness, heartburn, abdominal pain, constipation or associated symptoms (self-reported), but otherwise healthy will be chosen to participate in the study (see "4. Participant Definition"). Participants will be advised to discontinue any other oral supplement targeting the gut, including antibiotics, during the study and at least 3 months prior to.

Participants will be asked to complete the baseline survey on gut and skin health before the study starts.

Participants will also be asked to discontinue any additional soda consumption during the study.

Each day in the morning, for lunch, or in the afternoon, participants will drink one 12 fl oz. can of Poppi ACV prebiotic soda.

After 2 full weeks (day 14 of the study period) of drinking Poppi daily, participants will complete the 2-week follow up survey of gut and skin health.

After four weeks (day 28) of the study period, participants will complete the 4-week end-of-study follow up survey of gut and skin health. Making the whole study period four weeks.

The gut health surveys completed at baseline, week two and week four will be evaluated to determine the impact of Poppi ACV prebiotic soda on symptoms of poor gut health/digestion/IBS, including bloating, gas, heartburn, constipation and abdominal pain, as well as skin health.

Enrollment

38 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age: 18-45
  • Male or Female
  • Must be in generally good health
  • BMI under 35
  • Self-reported issues with gas, bloating, heartburn/acid reflux, abdominal pain or digestion
  • Willing to maintain their standard dietary pattern, activity level and body weight for the duration of the study

Exclusion criteria

  • Severe chronic conditions, including oncological conditions or psychiatric disease
  • Currently pregnant, wanting to become pregnant, or breastfeeding for the duration of the study
  • Taking any prescription medication targeting the gut
  • Taking any supplements targeting the gut in the past month
  • Use of antibiotics in the past 3 months

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

38 participants in 1 patient group

Poppi ACV prebiotic soda
Experimental group
Description:
Each day in the morning, for lunch, or in the afternoon, participants will drink one 12 fl oz. can of Poppi ACV prebiotic soda.
Treatment:
Dietary Supplement: Drink Poppi Soda

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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