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Evaluation of the Efficacy and Safety of Topical Adiponectin Peptides on Hair Growth and Preventing Hair Loss

Not Applicable
Recruiting
Conditions
Diseases of the skin and subcutaneous tissue
Registration Number
KCT0003559
Lead Sponsor
Seoul National University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
60
Inclusion Criteria

• volunteer in writing to participate who understand the need and process of clinical trials
• Among the men aged 18 to 49, Hamilton-Norwood class III, IV, V
• Volunteers who can follow-up during the trial period during the trial period

Exclusion Criteria

• If you have severe acute kidney or heart disease or other chronic illness that may affect your test results in the last 6 months
• Have experience with finasteride or other 5a-Reductase inhibitors within 12 months before screening.
• If you have experience using plant remedies (eg saw palmetto) within 8 weeks before screening
• Use of glucocorticoids within 3 months prior to screening (inhaled glucocorticoids allowed; topical steroids are allowed if not used on scalp)

• Usage 6 months before screening :
? Minoxidil (oral or topical)
? Drugs with antiandrogenic properties (eg cyproterone acetate, spironolactone, ketoconazole, flutamide, and bicalutamide). Cimetidine can not be used during the trial period, but it has not been used for the last 6 months.
? Local estrogen, progesterone
? Tamoxifen
? Drugs that can cause hyperhidrosis to cause hyperactivity (eg cyclosporine, diazoxide, phenytoin psoralens)
? Anabolic steroids
? Lithium and phenothiazine
• Use of past cytotoxic agents
• Simultaneous or regular use of topical agents on scalp for 4 weeks before screening
• Have received surgical treatment for hair loss such as hair transplantation or scalp reduction
• You have used other products that have been called "hairballs" within the last 3 months.
• Have recently taken or are currently taking medications that may affect hair growth
• If you are suffering from alopecia due to causes other than male hair loss
• Others who are unable to communicate or who are unable to follow instructions

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hair density
Secondary Outcome Measures
NameTimeMethod
mean hair diameter;linear hair growth rate;ratio of the anagen hair;non-vellus hair count
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