A Clinical Trial to Evaluate the Efficacy of ConcenTrace to Buffer pH Levels Within the Body.
Not Applicable
Completed
- Conditions
- pH
- Registration Number
- NCT06122597
- Lead Sponsor
- Trace Minerals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Inclusion Criteria:<br><br> - Male or female. Aged 18+. Generally healthy - don't live with any uncontrolled<br> disease. Willing to maintain their standard dietary pattern, activity level, and<br> body weight for the duration of the study.<br><br>Exclusion Criteria:<br><br> - Anyone with a pre-existing chronic condition that would prevent participants from<br> adhering to the protocol, including oncological and psychiatric disorders.<br><br>Anyone with known severe allergic reactions. Women who are pregnant, breastfeeding, or<br>attempting to become pregnant. Anyone unwilling to follow the study protocol.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in urine pH levels. [Timeframe: Baseline to Week 12]
- Secondary Outcome Measures
Name Time Method Change in score on the Metabolic Screening Questionnaire.