Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2020-03-05
2020-03-25
Brief Summary
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Detailed Description
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In a previous study using Delphinol® at various dosages, Delphinol® significantly and dose-dependently improved glucose homeostasis acutely, with noted lowering of blood glucose and lipids. The mechanism of action for this effect appears related to a novel sodium glucose cotransporter inhibition . This favorable effect on glucose and lipid metabolism is an effect that some have suggested may be associated with the protection of vascular function. A dosage of 450mg of Delphinol® daily has resulted in improvements in oxidative stress markers, another factor that can potentially contribute to vascular homeostasis. Together, these studies suggest Delphinol® may influence vascular function; however, no studies have directly determined this in human subjects.
Though similar studies exist demonstrating anthocyanin consumption resulting in improvements in vascular function, none to date have investigated different doses of a maqui extract on vascular function as assessed using the digital thermal monitoring of reperfusion. Digital thermal monitoring is suggested to be a more reliable measure of vascular function because it removes the sonographer variability; that is, accurately capturing the brachial artery with an ultrasound transducer can be very challenging.
The aim of the present study is to determine the impact of Delphinol® at varying dosages on vascular function assessed using the perfusion index, Vendys II (a tool to measure endothelial vascular function via digital thermal monitoring), and blood nitrate/nitrite concentrations in men and women. While it may be logical to assume that the higher dosage may provide a more robust overall effect with regards to our outcome measures, we will maintain a conservative non-directional hypothesis related to dose. That said, we do hypothesize that all doses of the ingredient will result in small improvements in the measured vascular indices.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
DOUBLE
Study Groups
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60mg Delphinol®
Capsule to be taken daily for 8 days
Delphinol
Contains maqui berry powder
120 mg Delphinol
Capsule to be taken daily for 8 days
Delphinol
Contains maqui berry powder
180 mg Delphinol
Capsule to be taken daily for 8 days
Delphinol
Contains maqui berry powder
Placebo
Capsule to be taken daily for 8 days
Placebo
Contains cellulose
Interventions
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Delphinol
Contains maqui berry powder
Placebo
Contains cellulose
Eligibility Criteria
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Inclusion Criteria
* male or female
* body mass index (BMI) between 18-29.9 kg/m2 (not obese)
* non-smoker
* no diagnosed history of diabetes
* no diagnosed history of cardiovascular disease including any vascular disease
* no diagnosed history of neurological disease
* no consumption of alcohol or fruit within 48 hours of testing
* no consumption of caffeine-containing beverages within at least 48 hours of testing
* 12-lead ECG without significant heart rate and rhythm abnormalities and blood glucose within normal limits (as reviewed by Tara Hunter, BSN and confirmed by Dr. John Hyden, MD as needed)
* if female, not be pregnant
18 Years
35 Years
ALL
Yes
Sponsors
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Anklam-Extrakt GmbH
UNKNOWN
University of Memphis
OTHER
Responsible Party
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Richard Bloomer
Dean of School of Health Studies
Principal Investigators
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Richard Bloomer, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Memphis
Locations
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Center for Nutraceutical and Dietary Supplement Research
Memphis, Tennessee, United States
Countries
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Other Identifiers
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PRO-FY2020-66
Identifier Type: -
Identifier Source: org_study_id
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