A Clinical Trial to Evaluate the Effect of ConcenTrace Trace Mineral Drops on Gut Health
- Conditions
- Gut HealthBowel MovementsBloatingConstipation
- Registration Number
- NCT06122571
- Lead Sponsor
- Trace Minerals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria:<br><br> - Be male or female. Be aged over 18. Have a BMI less than 35. Have issues with<br> digestion, heartburn, indigestion, gas, or constipation. Be willing to maintain<br> their standard dietary pattern, activity level, and body weight for the duration of<br> the study.<br><br>Be generally healthy - must not live with any uncontrolled disease.<br><br>Exclusion Criteria:<br><br> - Any person with a pre-existing chronic condition that might prevent the participant<br> from adhering to the protocol, including any oncological and psychiatric disorders.<br><br>Anyone taking any prescribed medication targeting the gut. Anyone taking any supplements<br>targeting the gut within the past month. Anyone with any known severe allergic reactions.<br>Women who are pregnant, breastfeeding, or attempting to become pregnant. Anyone unwilling<br>to follow the study protocol.
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in scores on the Gastrointestinal Symptom Rating Scale (GSRS). [Timeframe: Baseline to Week 12]
- Secondary Outcome Measures
Name Time Method Changes in stool consistency reported via the Bristol Stool Chart. [Timeframe: Baseline to Week 12];Changes in bowel movement frequency. [Timeframe: Baseline to Week 12]