Skip to content

Seaweed-derived Rhamnan Sulfate and Vascular Function

Seaweed-derived Rhamnan Sulfate and Vascular Function

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05651230
Enrollment
15
Registered
2022-12-14
Start date
2023-04-01
Completion date
2025-02-01
Last updated
2026-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases

Brief summary

The primary aim of the proposed investigation is to examine the hypothesis that a relatively short period of rhamnan sulfate supplementation would improve key markers of vascular dysfunction in middle-aged and older adults with at least one risk factors for cardiovascular disease.

Interventions

DIETARY_SUPPLEMENTRhamnan sulfate

A randomized, placebo-controlled, double-blind crossover dietary supplement intervention consisting of 3 weeks each of rhamnan sulfate (Rhamnox100, Konan Chemical Manufacturing Co. LTD, Mie, Japan: 540 mg/day) or placebo with 2 weeks of washout between the interventions will be conducted. Dietary supplements (rhamnan sulfate) will be taken orally three time daily at each meal time. Rhamnan sulfate is a polysaccharide (carbohydrate) extracted from seaweeds and can be considered nutrition supplement. As each pill contains 90 mg of rhamnan sulfate or placebo, subjects will be taking 2 pills before or during each meal.

Sponsors

University of Texas at Austin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* at least one risk factor for cardiovascular disease (e.g., dyslipidemia, hypertension, obesity, impaired fasting glucose) * a BMI of \<40 kg/m2

Exclusion criteria

* gastrointestinal disorders and/or renal disease * pregnancy or lactation * strenuous physical activity (\>3 times/week) * alcohol abuse

Design outcomes

Primary

MeasureTime frameDescription
Vascular functionBefore the 3-week interventionEndothelium-dependent vasodilation as assessed by flow-mediated dilation

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 10, 2026