Last updated: August 21, 2024
Sponsor: Trace Minerals
Overall Status: Completed
Phase
N/A
Condition
Constipation
Lactose Intolerance
Colic
Treatment
ConcenTrace
Clinical Study ID
NCT06122571
20351
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Be male or female. Be aged over 18. Have a BMI less than 35. Have issues withdigestion, heartburn, indigestion, gas, or constipation. Be willing to maintaintheir standard dietary pattern, activity level, and body weight for the duration ofthe study.
Be generally healthy - must not live with any uncontrolled disease.
Exclusion
Exclusion Criteria:
- Any person with a pre-existing chronic condition that might prevent the participantfrom adhering to the protocol, including any oncological and psychiatric disorders.
Anyone taking any prescribed medication targeting the gut. Anyone taking any supplements targeting the gut within the past month. Anyone with any known severe allergic reactions. Women who are pregnant, breastfeeding, or attempting to become pregnant. Anyone unwilling to follow the study protocol.
Study Design
Total Participants: 40
Treatment Group(s): 1
Primary Treatment: ConcenTrace
Phase:
Study Start date:
October 05, 2023
Estimated Completion Date:
January 31, 2024
Connect with a study center
Citruslabs
Santa Monica, California 90404
United StatesSite Not Available
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