TCTR20201104003
Recruiting
Phase 2
The study of clinical effectiveness and safety of a combination of 0.4% minoxidil and 0.05% retinaldehyde nanoparticles solution for treatment of androgenetic alopecia
ermatology division, Department of internal medicine, King Chulalongkorn Memorial Hospital0 sites30 target enrollmentNovember 4, 2020
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Androgenetic alopecia
- Sponsor
- ermatology division, Department of internal medicine, King Chulalongkorn Memorial Hospital
- Enrollment
- 30
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patient with androgenetic alopecia with Norwood\-Hamilton grade 3\-4 or Ludwig
- •2\.Volunteers who have well adherence and can be followed up as appointed grade 1\-2
Exclusion Criteria
- •1\.Prior treatment of androgenetic alopecia with topical therapy within 3 months
- •2\.Prior treatment of androgenetic alopecia with oral therapy within 6 months
- •3\.Prior treatment of androgenetic alopecia with hair transplantation within 12 months
- •4\.Pregnancy or breastfeeding
- •5\.Hirsutism
- •6\.Abnormal thyroid function
- •7\.Iron deficiency anemia
- •8\.Patient recieved contraception or hormone replacement therapy
Outcomes
Primary Outcomes
Not specified
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