The effectiveness and safety evaluation of hair growth promotor containing teak leaf extract
Not Applicable
Completed
- Conditions
- Hair growth promotor in men who suffer from androgenic alopeciaSkin and Connective Tissue Diseases
- Registration Number
- ISRCTN24541842
- Lead Sponsor
- ational Research Council of Thailand
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Male
- Target Recruitment
- 90
Inclusion Criteria
Men who suffered from androgenic alopecia defined by Hamilton-Norwood type II to V, age 20-60 years old.
Exclusion Criteria
1. A lesion on the scalp
2. Sensitivity to hair growth promotors or minoxidil
3. Use of other hair-regrowth products for 3 months and/or minoxidil for 6 months before enrolling in this project
4. Systemic steroids for more than 14 days within 2 months before baseline evaluation
5. Medical history of radiation on the scalp
6. Personal chronic decreases i.e. chronic kidney disease, and non-controlled blood pressure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Target area hair count (TAHC), hair density, anagen hair count, and telogen hair count were measured by macro-photography trichoscopy Leviacam at baseline and every 4 weeks for a total duration of 24 weeks <br>2. Hair shedding measured using a combing test macro-photography trichoscopy Levicam at baseline and every 4 weeks for a total duration of 24 weeks <br>3. Safety and adverse effects measured by a dermatologist evaluation at baseline and every 4 weeks for a total duration of 24 weeks <br>4. Hair growth satisfaction measured using a questionnaire at the end of the study (week 24)
- Secondary Outcome Measures
Name Time Method There were no secondary outcome measures