NCT01039662CompletedNot Applicable
Effects of the Combination of L-Arabinose and Indigestible Dextrin on Glycemic Index: a Double-Blind, Crossover Trial
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Hiroshima University
- Enrollment
- 19
- Locations
- 2
- Primary Endpoint
- Postprandial glucose level
Study Overview
Brief Summary
This study aims to investigate the effect of supplement containing L-arabinose and indigestible dextrin on dietary glycemic index.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover
- Primary Purpose
- Prevention
- Masking
- Double (Participant, Outcomes Assessor)
Eligibility Criteria
- Ages
- 20 Years to 50 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Healthy as based on medical history and physical examination
- •BMI is less or equal to 30 kg/m2
- •Willing not to serve as blood donor during the study
- •Informed consent signed
Exclusion Criteria
- •Impaired Glucose Tolerance
- •Female subjects who are pregnant or nursing a child
- •Participation in any clinical trial up to 90 days before Day 1 of this study
- •Renal or hepatic dysfunction
- •Heart disease
- •Under medication
Arms & Interventions
Oolong tea containing L-arabinose and indigestible dextrin
Experimental
Intervention: L-arabinose and indigestible dextrin (Dietary Supplement)
Oolong tea
Placebo Comparator
Intervention: Placebo (Dietary Supplement)
Outcomes
Primary Outcomes
Postprandial glucose level
Time Frame: 2 hours
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (2)
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