A Clinical Trial to Evaluate the Efficacy of ConcenTrace to Buffer pH Levels Within the Body.
NCT ID: NCT06122597
Last Updated: 2024-08-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2023-10-05
2024-01-31
Brief Summary
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Urine pH measurements will be taken at Baseline, Week 4, Week 8, and Week 12 using pH test strips.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Test arm: ConcenTrace
Participants should follow this weekly dosing schedule:
Week 1 - Days 1-3: take 5 drops of ConcenTrace with 8 oz of water or flavored water. Days 4-7: take 5 drops of ConcenTrace 2x daily with 8 oz of water or flavored water.
Week 2: Take 10 drops of ConcenTrace 2x daily with 8 oz of water or flavored water.
Week 3: Take 15 drops of ConcenTrace 2x daily with 8 oz of water or flavored water.
Weeks 4-12: Take 20 drops of ConcenTrace 2x daily with 8 oz of water or flavored water.
ConcenTrace
The product contains concentrated seawater from Utah's inland sea.
Interventions
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ConcenTrace
The product contains concentrated seawater from Utah's inland sea.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
Anyone with known severe allergic reactions. Women who are pregnant, breastfeeding, or attempting to become pregnant. Anyone unwilling to follow the study protocol.
18 Years
ALL
Yes
Sponsors
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Citruslabs
INDUSTRY
Trace Minerals
INDUSTRY
Responsible Party
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Locations
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Citruslabs
Santa Monica, California, United States
Countries
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Other Identifiers
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20352
Identifier Type: -
Identifier Source: org_study_id
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