Prospective Safety and Tolerability Assessment of a Cardiovascular Health Dietary Supplement



Status:Completed
Conditions:High Blood Pressure (Hypertension)
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - 65
Updated:4/17/2018
Start Date:May 1, 2015
End Date:July 28, 2017

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This single-arm, open-label study will assess the safety and tolerability of one daily tablet
of a commercially available cardiovascular health dietary supplement by questionnaire and
blood markers in adults with borderline to mild hypertension over a 6 month period. Although
the cardiovascular health dietary supplement being investigated has been on the market for
over 20 years, prospective safety data and blood markers of end organ function have not
previously been reported.

Hypertension is an important overall risk factor for developing cardiovascular disease in the
United States, and is a leading risk factor for cardiovascular events, including myocardial
infarction and stroke, and cardiovascular-related mortality with advancing age. Based on
population based studies and clinical trials, both systolic blood pressure (SBP) and
diastolic blood pressure (DBP) elevations are continuous, strong and independent risk factors
for cardiovascular disease.

The product being studies is a cardiovascular health dietary supplement that has been
commercially available since 1993. It is currently sold to healthcare practitioners as well
as directly to consumers. Some healthcare providers use the product as part of a plan to
treat high blood pressure in their patients. This is the first study collecting prospective
safety data on this product.

Inclusion Criteria:

- Age 18-65

- Systolic blood pressure 120-159 mmHg or diastolic blood pressure 80-99 mmHg upon
screening

Exclusion Criteria:

- Bradycardia

- Initiation of or changes to blood pressure lowering medications within the last month

- Initiation of or changes to thyroid medications within the last month

- Currently taking any of the following orally (or they were taken within the last
month):

- Rauwolfia serpentina, Terminalia arjuna, Tribulus terrestris, Convolvulus
pluricaulis, Boerhavia diffusa, Rosa vinca, rose powder, or coral powder

- Beta blockers

- Alpha blockers

- Propranolol

- Digoxin

- Levodopa

- Anti-depressant medications

- Anti-psychotic medications

- Sedatives or tranquilizers

- Present or past history of any of the following:

- Cardiovascular disease

- Heart surgery

- Cardiac arrhythmia

- Abnormal EKG

- Abnormal echocardiogram

- Diabetes

- Chronic liver, kidney or bowel disease

- Ulcers

- Gallbladder disease

- Depression

- Alcoholism

- Obstructive sleep apnea and/or use of a continuous positive airway pressure
device

- Parkinson's disease

- Pheochromocytoma

- Cancer within the last 5 years

- Consuming more than fourteen alcoholic beverages per week

- Current smoking/tobacco use

- Current illicit and/or recreational drug use

- Women who are lactating, pregnant or planning pregnancy within the next six months

- Known intolerance or allergy to study agents
We found this trial at
1
site
2220 Southwest 1st Avenue
Portland, Oregon 97201
?
mi
from
Portland, OR
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