Clinical Test Report for improving hair loss of 2 Cosmetics

Not Applicable

Completed

• Conditions: Diseases of the skin and subcutaneous tissue

• Registration Number: KCT0005501
• Lead Sponsor: Seowon University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2021-05-20
• Last Update Posted: 30 August 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 48

Inclusion Criteria

Volunteer between the ages of 18 and 54 diagnosed with androgenic hair loss.
- Patients who will not have special hair products or hair care and manipulation during the study period
- Patients who will maintain the same head shape for the duration of the study.
- Volunteer who understands the research and voluntarily prepares and signs a consent form to participate in clinical trials.
- Volunteer who can be monitored during a test period

Exclusion Criteria

- Volunteer suffering from severe acute kidney or heart or other chronic diseases (hypertension, diabetes, etc.) that may affect test results in the last six months.
- Volunteer who is pregnant, breast-feeding, or planning to conceive within six months.
- A mentally ill person
- Volunteer with an infectious skin condition
- Volunteer who has undergone surgical treatment for hair loss, such as hair transplantation, scalp reduction, etc.
- Those who have been taking the following drugs for the past month: steroids, apoptosis, vascular dilators, anticoagulants, anticorruption agents, beta receptor blockers, bronchial extensions, diuretics, diazoxide, cyclosporine, ketomonazole
- Volunteer who has been applying local steroid preparations to the scalp for the past month.
- Volunteer who is deemed to have difficulty in applying the test substance due to severe seborrheic dermatitis, psoriasis of the scalp, or infection of the scalp.
- In addition to androgenic hair loss, patients with other hair loss diseases such as circular hair loss, tissue hair loss, and semitransparent hair loss.
- Any other person deemed unfit for the examination by the person in charge of research.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
Hair density

Secondary Outcome Measures

Name	Time	Method
Researcher evaluation by photography;Survey evaluation by test subjects