Efficacy Testing of Hibiscus Sabdariffa Extract and Collagen Products
NCT ID: NCT05988554
Last Updated: 2024-02-21
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
50 participants
INTERVENTIONAL
2023-06-05
2023-12-31
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
OTHER
DOUBLE
Study Groups
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Placebo sachet
Placebo sachet
Consume 1 sachet daily
Hibiscus sabdariffa extract and collagen products
Hibiscus sabdariffa extract and collagen products
Consume 1 sachet daily
Interventions
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Placebo sachet
Consume 1 sachet daily
Hibiscus sabdariffa extract and collagen products
Consume 1 sachet daily
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients with diseases of the skin, liver, kidney.
* 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 (\> 3 hr/week) in the past 4 weeks.
* Constant drug use
* Students who are currently taking courses taught by the principal investigator of this trial.
20 Years
ALL
Yes
Sponsors
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TCI Co., Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Chia-Hua Liang
Role: PRINCIPAL_INVESTIGATOR
Chia Nan University of Pharmacy ＆ Science
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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23-048-B
Identifier Type: -
Identifier Source: org_study_id
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