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Anti-pollution Effects of AP Green Tea Extracts

A

Amorepacific

Status

Completed

Conditions

Respiratory Conditions Due to Unspecified External Agent

Treatments

Dietary Supplement: AP green tea extracts

Study type

Interventional

Funder types

Industry

Identifiers

NCT04340375
AP-R-2018-01

Details and patient eligibility

About

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

Enrollment

40 patients

Sex

All

Ages

19 to 70 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

AP green tea extracts
Experimental group
Description:
8 weeks
Treatment:
Dietary Supplement: AP green tea extracts

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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