A Clinical Trial to Evaluate the Effect of ConcenTrace Trace Mineral Drops on Gut Health

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

This is a virtual single-arm trial that will last 12 weeks. Participants will take the drops daily and complete questionnaires at Baseline, Week 4, Week 8, and Week 12. Gut health, bowel movements, stool looseness, constipation, bloating, and regularity will be evaluated at the Baseline and at each check-in. Likert scale responses will be statistically compared from Baseline to each check-in. Participant responses and product feedback will be presented as percentage scores.

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 States

    Site Not Available

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