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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03118167
Other study ID # RCT-001-AA
Secondary ID
Status Completed
Phase N/A
First received November 24, 2016
Last updated May 16, 2017
Start date May 2014
Est. completion date December 2014

Study information

Verified date May 2017
Source Zhejiang University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A double-blind randomized controlled trial (RCT) was conducted in current human study. This study aims to investigate the intervention effect of AOB-w on the short-term exposure and toxicokinetics of acrylamide, a dietary hazardous substance generated during heat processing, in Chinese adolescents.


Description:

In the morning of test day, participants were served with a meal of potato chips, corresponding to a single oral dose of 12.6 μg/kg b.w. exposure to acrylamide, and an edible capsule, which contains 350 mg AOB-w or the placebo with the same dose. Urine were collected within 48 hours thereafter. The diet was rigorously controlled within 24 hours prior to study till entire study finished. Four mercapturic acid metabolites have been investigated as urinary biomarkers for short-term internal exposure of acrylamide in human


Recruitment information / eligibility

Status Completed
Enrollment 110
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 17 Years to 29 Years
Eligibility Inclusion Criteria:

- Subject has no smoking or drinking hobby

Exclusion Criteria:

- Having any drugs within 7days

- Smoking or drinking

- Pregnant, trying to become pregnant or breast feeding

- Allergic frying foods

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Tea polyphenols
Tea polyphenols 0.05g, 0.1g, 0.2g (starches filled up to 0.35g), edible capsule
AOB-w
Water-soluble antioxidant of bamboo leaves 0.35g, edible capsule
Other:
Placebo
Edible starches 0.35g, edible capsule
Acrylamide (Potato Chips)
Potato Chips bought from market, corresponding to acrylamide (12.6µg/kg b.w. )

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Zhejiang University

Outcome

Type Measure Description Time frame Safety issue
Primary Change of four urinary biomarkers of acrylamide Urine was collected prior to the potato chips meal and 48 hours thereafter, up to 10 urine samples for each participants. Urinary biomarkers of acrylamide were detected by UHPLC-MS/MS. up to 48 hours
Primary Change of two hemoglobin adducts of acrylamide Blood samples were collected in 0, 3, 10days after the intake of potato chips meals. Two hemoglobin adducts (AAVal and GAVal) of acrylamide were detected by UHPLC-MS/MS. baseline, 3 and 10 days
Secondary Area under the concentration versus time curve (AUC) Of acrylamide urinary biomarkers Dynamic changes of biomarkers during the specified intervention period, following 10 urine samples in 48 hours thereafter. baseline, 2, 4, 6, 8, 10, 14, 24, 36 and 48 hours
Secondary Maximum Concentration (Cmax) of Acrylamide Urinary Biomarkers Maximum concentration of urinary biomarkers during the specified period, measured by curve fitting tools of Matlab Software. 48 hours
Secondary Time to Peak Concentration (tmax) of Acrylamide Urinary Biomarkers Time to Peak Concentration (tmax) of Acrylamide Urinary Biomarkers during the specified period, measured by curve fitting tools of Matlab Software. 48 hours
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