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Clinical Trials/TCTR20201104003
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.

Registry
who.int
Start Date
November 4, 2020
End Date
May 31, 2021
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
ermatology division, Department of internal medicine, King Chulalongkorn Memorial Hospital

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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