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The safety and efficacy of topical Dutasteride in comparison to topical Dutasteride & laser therapy in management of female pattern hair loss

The safety and efficacy of topical Dutasteride in comparison to topical Dutasteride & laser therapy in management of female pattern hair loss

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241003063247N1
Enrollment
40
Registered
2024-12-02
Start date
2024-11-18
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Female pattern hair loss. Other androgenic alopecia

Interventions

Intervention 1: First interventional group: Dutasteride solution 60/ml which contain the active ingredient Dutasteride with a concentration of 0.1% mg/ml was prepared by pharmacists in Tasnim Pharmace

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Age more than 18 year old clinical and trichoscopic diagnosis of female pattern hair loss female patients Female pattern hair loss grade 1-3 ludwig scale

Exclusion criteria

Exclusion criteria: Past history of treatment of AGA in the last three months Alcoholism or addicted Past history of hair transplant systemic diseases or dermatological diseases that may affect hair regrowth Sensitivity to topical dutasteride Sexual dysfunction Current treatment for AGA Lactation and pregnancy

Design outcomes

Primary

MeasureTime frame
Number and percentage of terminal and vellous hair, in addition to diameter of the hair terminals. Timepoint: Number and percentage of terminal and vellous hair, in addition to diameter of the hair terminals before intervention, 3 months after intervention and lastly 6 months after intervention. Method of measurement: Trichoscopy.

Secondary

MeasureTime frame
Overall increase in hair density. Timepoint: initially, after 3 months and lastly after 6 months. Method of measurement: trichscopy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaman Alzahawi

Tehran University of Medical Sciences

samanzahawi88@gmail.com+98 922 625 6180

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026