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Clinical Trials/NCT01162174
NCT01162174CompletedPhase 1

Effects of Oligonol on Vascular Function and Inflammation in Healthy Men: A Double-Blind, Dose-Finding Study

University of California, Davis0 sites16 target enrollmentStarted: August 1, 2008Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
16
Primary Endpoint
Peripheral Arterial Tonometry

Study Overview

Brief Summary

The investigators hypothesize that acute consumption of Oligonol, a patented lychee fruit extract (Amino Up Chemical Co.) particularly rich in low molecular weight flavanols, will improve endothelial function, reduce platelet reactivity and increase circulating levels of flavonoids after a single intake.

Detailed Description

The investigators have demonstrated from previous studies at UC Davis that a single dose of a high-flavanol supplement from cocoa can improve endothelial function, measured by increased blood flow from peripheral arterial tonometry (PAT), reduce platelet reactivity, and increase circulating levels of flavonoids in the blood. The investigators seek with this proposal to determine if a similar response can be noted with a different high-flavanol supplement in normal, healthy people.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Age 18-50 yrs.
  • •Healthy, not taking prescription medications
  • •Subject is willing and able to comply with the study protocols.
  • •Subject is willing to consume the Oligonol extract drink or placebo once a week for each of three weeks.

Exclusion Criteria

  • •Physical signs of health impairment.
  • •Abnormal clinical laboratory (CBC, chemistry, liver, etc.) values if determined to be clinically significant by Dr. Eric Gershwin
  • •Inflammatory disorders (e.g. rheumatoid arthritis)
  • •Malabsorption
  • •Treatment with corticosteroids, hypolipidemic and anti-inflammatory drugs
  • •Renal or Liver disease
  • •Heart Disease, which includes cardiovascular events and stroke
  • •Cushing's syndrome
  • •History of psychiatric disorders i.e. schizophrenia or bi-polar or depression treated with antidepressants within the last 1 year.
  • •Anti-anxiety medications
  • •Routine use of prescription drugs or over-the counter medications, which may potentially modulate the outcome of this study; including antibiotics, aspirin and aspirin-containing formulations, COX-2 inhibitors, antihistamines, corticosteroids, ACE-inhibitors, and beta-blockers, erectile dysfunction drugs.
  • •Asthma (can be worsened by mild to moderate food allergies).
  • •Indications of substance or alcohol abuse within the last 3 years
  • •Undergoing nicotine cessation therapy
  • •Multi-Vitamin and mineral use other than a One-A-Day type formula
  • •Current, consistent use of herbal or plant-based supplements; omega-3 fatty acids, and fish or unwilling to discontinue use while participating in the study.
  • •Alcohol consumption > 1 oz/day (2 beers/day or 2 glasses of wine/ day, 1 drink of hard liquor/day)
  • •Chronic high-intensity exercise

Arms & Interventions

100 mg of Oligonol

Experimental

Intervention: Oligonol (Dietary Supplement)

200 mg of Oligonol

Experimental

Intervention: Oligonol (Dietary Supplement)

0 mg of Oligonol

Placebo Comparator

Intervention: Oligonol (Dietary Supplement)

Outcomes

Primary Outcomes

Peripheral Arterial Tonometry

Time Frame: 0 and 2 hours

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

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