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Clinical Trials/NCT00781534
NCT00781534CompletedEarly Phase 1

A Clinical Trial of Ginseng for Glucose Intolerance

Washington University School of Medicine1 site in 1 country19 target enrollmentStarted: September 2003Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Early Phase 1
Status
Completed
Enrollment
19
Locations
1

Study Overview

Brief Summary

a clinical study of Ginseng its potential affect on diabetes

Detailed Description

Comparing three groups (those with & without normal blood sugar levels) to see if there is any clinically significant change in blood sugar levels in relationship to those taking:

  1. ginseng
  2. ginsenoside RE (a type of metabolized ginseng)
  3. placebo

Study Design

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

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • ages 18-65
  • healthy, non-diabetic
  • healthy, impaired glucose tolerance/mild diabetes (no medications required)

Exclusion Criteria

  • impaired glucose tolerance (borderline diabetes that requires medications)
  • diabetes (requiring medications)
  • caffeine sensitivity
  • known cardiac, peripheral vascular diseases
  • arrhythmias (irregular heart rhythms)

Arms & Interventions

1. Ginseng

Active Comparator

Ginseng group

Intervention: Ginseng (Drug)

2. Ginsenosdie RE

Active Comparator

Ginsenoside RE (a metabolite of ginseng) group

Intervention: Ginseng (Drug)

2. Ginsenosdie RE

Active Comparator

Ginsenoside RE (a metabolite of ginseng) group

Intervention: ginsenoside RE (Drug)

3. Placebo

Placebo Comparator

placebo ("sugar" pill) group

Intervention: Placebo (sugar pill) (Dietary Supplement)

Investigators

Study Sites (1)

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