Skip to content

Efficacy of Dihydroartemisinin for Treating Female Androgenetic Alopecia

A Pilot Study to Evaluate the Therapeutic Effect of Dihydroartemisinin on Female Androgenetic Alopecia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07012486
Enrollment
30
Registered
2025-06-10
Start date
2025-06-30
Completion date
2026-12-31
Last updated
2025-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Androgenetic Alopecia (AGA)

Keywords

androgenetic alopecia, dihydroartemisinin

Brief summary

The goal of this clinical trial is to learn if dihydroartemisinin (DHA) works to treat Androgenetic Alopecia (AGA) in female adults. The main question it aims to answer is: • Does DHA increase terminal hair follicles in the vertex area. Researchers will compare oral DHA plus topical minoxidil to topical minoxidil alone in female patients with AGA to see if DHA works to alleviate AGA. Participants will: * Receive oral DHA every day plus topical minoxidil or use topical minoxidil alone for 6 months. * Visit the clinic once every month for checkups and tests.

Interventions

DRUGOral DHA + Topical minoxidil 5%

DHA 20mg tid po plus daily topical minoxidil 5% for 180 days

Topical minoxidil 5% daily for 180 days

Sponsors

Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Clinically diagnosed with androgenetic alopecia (AGA) * No pregnancy plans within the next 6 months

Exclusion criteria

* Patients who received systemic medications for hair loss within the past 2 months * Use of topical medication for hair loss within the past 2 weeks * Pregnancy or lactation * Patients with known severe diseases of vital organs (e.g., heart, liver, kidney) or malignancies.

Design outcomes

Primary

MeasureTime frameDescription
Improvement in terminal hair follicles in the vertex areaBaseline and 180-day of treatmentTerminal hair follicles in the vertex area will be quantified before and at the end of treatment

Secondary

MeasureTime frameDescription
Change of terminal hair follicle density in the vertex area from baseline to the end of treatmentBaseline and 180-day of treatment
Change of hair density in the vertex area from baseline to the end of treatmentBaseline and 180-day of treatment
Change of terminal hair follicle density in the frontal area from baseline to the end of treatmentBaseline and 180-day of treatmentTerminal hair follicle density in the frontal area
Change of hair density in the frontal area from baseline to the end of treatmentBaseline and 180-day of treatment
Change of serum total testosterone from baseline to the end of treatmentBaseline and 180-day of treatment

Countries

China

Contacts

Primary ContactLujuan GAO, MD, PhD
gao.lujuan@zs-hospital.sh.cn86-021-64041990

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026