Safety and Tolerability of 2 Dietary Supplement Beverages Designed to Maintain Healthy Blood Pressure.

Part of paid clinical trials in Salt Lake City, Utah.

Sponsor
USANA Health Sciences
Study ID
NCT06442293
Status
Not Yet Recruiting

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Conditions

  • Safety Issues
  • Tolerance

Eligibility Criteria

Sex
ALL
Age
18 Years - 50 Years
Healthy Volunteers
Accepted

Interventions

  • Treatment 1 — DIETARY_SUPPLEMENT
    A dietary supplement containing beet root extract, arginine and citrulline
  • Treatment 2 — DIETARY_SUPPLEMENT
    A traditional Chinese medicine (TCM)-based dietary supplement containing chrysanthemum extract and eucommia bark extract
  • Placebo — DIETARY_SUPPLEMENT
    a placebo supplement that is similar in appearance to treatment 1

Study Details

This study is designed to evaluate the safety and tolerability of two distinct dietary supplement beverage formulations designed to maintain normal blood pressure. In this study, safety and tolerability will be assessed among otherwise healthy, normotensive individuals.

Key Dates

Start date
Jul 1, 2024
Status verified
Jun 2024
Primary completion
Aug 15, 2024
Completion
Aug 15, 2024

Study Design

Enrollment
18 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Placebo Comparator: Placebo
    a placebo (microcrystalline cellulose) identical in size, shape and color to the treatment
  • Experimental: Circulatory Beverage - low dose
    A beverage containing natural ingredients at a low dose
  • Experimental: Circulatory Beverage - medium dose
    A beverage containing natural ingredients at a medium dose
  • Experimental: Circulatory Beverage - high dose
    A beverage containing natural ingredients at a high dose
  • Experimental: TCM Beverage - low dose
    A traditional Chinese medicine-based beverage containing natural ingredients at a low dose
  • Experimental: TCM Beverage - high dose
    A traditional Chinese medicine-based beverage containing natural ingredients at a high dose

Primary Outcome Measure

Aggregate Adverse Symptom Score [ Time Frame: 4 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
USANA Health SciencesSalt Lake CityUtah84120-

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