Supplementation Absorption Comparison
NCT07791797 · Status: NOT_YET_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 160
Last updated 2026-08-28
Summary
The goal of this interventional study is to compare the absorption of supplements with and without absorption enhancing technology in healthy volunteers. We will be testing vitamin D3 and omega 3 in both males and females 18 years and older. Part A will comprise of two arms receiving a single dose of omega-3 supplement, and two arms who will receive vitamin D3 supplement daily for 7 days. Part B comprises of two arms who will receive vitamin D3 supplement daily for 6 weeks.
Conditions
- Healthy Volunteer
Interventions
- DIETARY_SUPPLEMENT
-
Aquacelle® Omega 3
Participants will consume 1 capsule containing 315mg EPA and DHA
- DIETARY_SUPPLEMENT
-
Comparator Omega 3
Participants will consume 1 capsule containing 315mg EPA and DHA
- DIETARY_SUPPLEMENT
-
Plexosome® Vitamin D3
Participants will have 1000IU vitamin D3 each day for 7 days
- DIETARY_SUPPLEMENT
-
Comparator Vitamin D3
Participants will have 1000IU vitamin D3 each day for 7 days
- DIETARY_SUPPLEMENT
-
Plexosome® Vitamin D3 6 weeks
Participants will have 1000IU vitamin D3 each day for 6 weeks
- COMBINATION_PRODUCT
-
Comparator Vitamin D3 6 weeks
Participants will have 1000IU vitamin D3 each day for 6 weeks
Sponsors & Collaborators
-
RDC Clinical Pty Ltd
lead INDUSTRY
Principal Investigators
-
David Briskey · RDC Clinical
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-09-30
- Primary Completion
- 2027-09-30
- Completion
- 2027-09-30
Countries
- Australia
Study Locations
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