Effects of Effera Human Lactoferrin at One Dose Compared to Placebo on Gut Permeability
Part of paid clinical trials in Addison, Illinois.
- Sponsor
- Helaina Inc.
- Study ID
- NCT07035964
- Status
- Recruiting
Conditions
- Gut Health
- Gut Permeability
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 40 Years
- Healthy Volunteers
- Accepted
Interventions
- human lactoferrin — DIETARY_SUPPLEMENTeffera human lactoferrin
- Placebo — DIETARY_SUPPLEMENTPlacebo Control
Study Details
The purpose of this study is to evaluate the impact of 28-day supplementation with effera human lactoferrin, compared to a placebo control product on indicators of gut barrier health in males and females
Key Dates
- Start date
- Jun 4, 2025
- Status verified
- Jun 2025
- Primary completion
- Aug 30, 2025
- Completion
- Aug 30, 2025
Study Design
- Enrollment
- 46 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: Dietary supplement: effera human lactoferrinDietary supplement: effera human lactoferrin
- Placebo Comparator: Dietary Supplement: Placebo ControlDietary Supplement: Placebo Control
Primary Outcome Measure
lactulose to mannitol ratio [ Time Frame: 0, 4 weeks ]
Central Contacts
- Ross Peterson, Ph.D.7204097993
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Biofortis Inc | Addison | Illinois | 60101 |
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