A Clinical Trial to Assess the Effect of a Combined Pre-, Pro-, and Post-biotic Supplement on Gut and Metabolic Health

Beekeeper's Naturals

Status

Completed

Conditions

Gut Health

Treatments

Other: Combined pre-, pro-, and post-biotic supplement

Study type

Interventional

Funder types

Industry

Identifiers

NCT05876845

20291 (Other Identifier)

Details and patient eligibility

About

This is a virtual, single-arm clinical trial that will last 4-weeks. Participants will take the supplement daily and complete questionnaires at baseline, week 2, and week 4. Participants will provide photos of their face and stomach at baseline and week 4.

Gut health and associated health outcomes, including brain, skin, and immune function, will be evaluated at baseline and at each check-in. Likert scale responses will be statistically compared from baseline to each check-in. Participant responses on product feedback will be presented as % scores. Baseline and endline photos from each study part will be provided by participants.

Enrollment

38 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Men or women
18 years of age or older
Experience at least one of the following symptoms: regular bloating/gas, irregular bowel movements, heartburn, or poor digestive health
Generally healthy

Exclusion criteria

Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders.
Allergic to bees, bee products, poplar tree products, or balsam of Peru
Anyone with known severe allergic reactions.
Women who are pregnant, breastfeeding or attempting to become pregnant
Unwilling to follow the study protocol.
Has introduced any new forms of medication or supplements targeting gut health within the last 3 months
Has taken antibiotics in the last 3 months