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Seaweed-derived Rhamnan Sulfate and Vascular Function

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Cardiovascular Diseases

Treatments

Dietary Supplement: Rhamnan sulfate

Study type

Interventional

Funder types

Other

Identifiers

NCT05651230
STUDY00003693

Details and patient eligibility

About

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.

Enrollment

15 estimated patients

Sex

All

Ages

35 to 85 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

15 participants in 2 patient groups, including a placebo group

Rhamnan sulfate
Experimental group
Description:
The subjects will take rhamnan sulfate (Rhamnox100, Konan Chemical Manufacturing Co. LTD, Mie, Japan: 540 mg/day) orally three time daily at each meal time.
Treatment:
Dietary Supplement: Rhamnan sulfate
Placebo
Placebo Comparator group
Description:
The subjects will take placebo (Konan Chemical Manufacturing Co. LTD, Mie, Japan: 540 mg/day) orally three time daily at each meal time.
Treatment:
Dietary Supplement: Rhamnan sulfate

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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