MedPath

A home use test of scalp lotions

Not Applicable
Conditions
Healthy adults
Registration Number
JPRN-UMIN000046486
Lead Sponsor
SOUKE
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
Female
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

-Subjects with suspected skin allergy, cutaneous hypersensitivity -Subjects with severe hay fever -Subjects who could cause skin allergy by shampoo, hair conditioner or scalp lotion -Subjects whose skin turns red with ethanol -Subjects with external injury, surgical treatments on test area -Subjects with atopic dermatitis, seborrheic dermatitis on test area -Subjects with highly exposed to sun light -Subjects whose hair was chemically treated within one week before the start of this study -Subjects who have rapid hair loss or hair missing in a patchy shape -Subjects who use pharmaceuticals, hair growth agents, tonics, moisturizers, etc. on the scalp -Subjects who regularly take vitamins and other supplements that can exhibit anti-inflammatory and dandruff-related efficacy -Subjects who use products containing carbon dioxide (shampoos, hair conditioners, etc.) on the scalp -Subjects who are pregnant or willing to become pregnant or are breastfeeding during the period of participation -Subjects who are going to the hospital or taking medication due to chronic illness -Subjects who have had strong symptoms such as shortness of breath (difficulty breathing), strong fatigue, or high fever within the past 2 weeks -Subjects who are considered to have had close contact with a COVID-19 patient from the public health center -Subjects who have get a COVID-19 vaccine within the past one week. -Subjects or her family members work for a company related to the manufacture and sale of pharmaceuticals, cosmetics, toiletry products, etc. -Subjects who participate in other surveys or studies -Subjects who plan to participate in other studies or surveys during the study period -Subjects deemed inappropriate to participate in this study by the person involved in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation of the dandruff and scalp dryness before and after use of scalp lotions for 4 weeks
Secondary Outcome Measures
NameTimeMethod
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