Anti-pollution Effects of AP Green Tea Extracts

NCT ID: NCT04340375

Last Updated: 2021-06-16

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-03

Study Completion Date

2020-04-30

Brief Summary

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The objective of this clinical trial is to evaluate the anti-pollution effects of AP green tea extracts in subjects with discomforts related to the respiratory system by prolonged exposure to particulate matter in air pollution

Detailed Description

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Conditions

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Respiratory Conditions Due to Unspecified External Agent

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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AP green tea extracts

8 weeks

Group Type EXPERIMENTAL

AP green tea extracts

Intervention Type DIETARY_SUPPLEMENT

AP green tea extracts

Interventions

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AP green tea extracts

AP green tea extracts

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Subjects aged 19 years or over
* Subjects with discomforts related to the respiratory system by prolonged exposure to particulate matter in air pollution
* Subjects who voluntarily decide to participate in this clinical study and sign the informed consent form on their own or through their representatives

Exclusion Criteria

* At the screening visit, subjects who were diagnosed with acute or chronic respiratory disease and undergoing medication.
* Subjects who were diagnosed with ventricular associated disease, unstable and uncontrolled chronic medical disease, or active malignant tumor and undergoing medication within 4 weeks prior to the first administration of the investigational product
* Subjects who show a level of ALT/AST of 2 times or more the upper limit of normal as a result of a screening test and have acute or chronic hepatitis or known liver cirrhosis
* In addition to the above, subjects who are determined to be ineligible to participate in the clinical study according to the investigator's medical opinion
Minimum Eligible Age

19 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Amorepacific Corporation

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hanyang University Seoul Hospital

Seoul, , South Korea

Site Status

Countries

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South Korea

Other Identifiers

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AP-R-2018-01

Identifier Type: -

Identifier Source: org_study_id

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