Investigation of the Efficacies of a Resveratrol Formula on Improvement of Skin Conditions and Inflammatory Related Factors
NCT ID: NCT04456829
Last Updated: 2021-01-15
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
60 participants
INTERVENTIONAL
2020-09-17
2020-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Resveratrol drink
Resveratrol drink
Subjects will consume a bottle of resveratrol drink for two months.
Placebo drink
Placebo drink
Subjects will consume a bottle of placebo drink for two months.
Interventions
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Resveratrol drink
Subjects will consume a bottle of resveratrol drink for two months.
Placebo drink
Subjects will consume a bottle of placebo drink for two months.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients with diseases of the skin, heart, liver, kidney, endocrine and other organs and patients with mental illness (according to medical history).
* Subjects who have known cosmetic, drug or food allergies, difficulty in digestive tract absorption or disorder.
* Female who is pregnant or nursing or planning to become pregnant during the course of the study.
* Received facial laser therapy, chemical peeling or UV overexposure in the past 4 weeks.
* Subjects who have large spots (area \>3 square centimeter) or abnormal acne.
20 Years
ALL
Yes
Sponsors
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TCI Co., Ltd.
INDUSTRY
Responsible Party
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Locations
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Chia Nan University of Pharmacy & Science
Tainan City, , Taiwan
Countries
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Other Identifiers
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20-0-54-B
Identifier Type: -
Identifier Source: org_study_id
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