A clinical study of body odor for test product

Not Applicable

Completed

• Conditions: Not Applicable

• Registration Number: KCT0003498
• Lead Sponsor: Dermapro

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 March 2019

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 22

Inclusion Criteria

1.Non-smoker, Healthy male and females; 50 to 61 years of age
2.The subject is apprised regarding the purpose and the protocol of the study; signed informed consent is obtained
3.Volunteers should be cooperative and available for follow-up during the study period

Exclusion Criteria

1.Pregnancy or nursing condition
2.Use of anti-inflammatories, corticoids, steroid within 1 month
3.Participation in a previous study without an appropriate intervening period (three months) between studies
4.Sensitivity or hypersensitivity skin
5.Subjects having marks, blemishes or nevi or presenting with existing sun damage in the test area
6.A chronic sickness (diabetes, asthma, high blood-pressure)
7.Atopic dermatitis
8.Any difficult which may interfere with the aim of the study as the judgement of the investigator

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Sensory evaluation of body odor test;Gas chromatography–mass spectrometry(GC/MS) analysis;Quantitative analysis of odor molecule by zNose®

Secondary Outcome Measures

Name	Time	Method
Electroencephalography(EEG) & Electromyography(EMG) measurement;Evaluation of axillary microbe