Skip to content

Saftey and Efficacy of alternate day regimen of Oral Dutasteride in male patients with Androgenic Alopecia

An Open label, Randomized, Non-inferiority Pilot study to evaluate the efficacy of daily and alternate day regimen of Oral Dutasteride in male patients with Androgenic Alopecia - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068777
Enrollment
80
Registered
2024-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: L649- Androgenic alopecia, unspecified

Interventions

Intervention1: Dutasteride: 0.5mg Oral Dutasteride to be given Alternate Day for 6 months Control Intervention1: Dutasteride: 0.5mg Oral Dutasteride to be given Once Daily for 6 months

Sponsors

Dr Neil Patel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Clinically diagnosed patients of androgenic alopecia not on any treatment in past 3 months 2. Patients willing to follow instruction and give informed consent

Exclusion criteria

Exclusion criteria: 1. Previous allergic reactions to finasteride like compounds 2. Prior surgical correction of scalp hair loss 3. Patients with any other inflammatory/scarring lesion on scalp 4. Patients with chronic systemic illness (Tuberculosis, HIV) 5. Patients on drugs with significant interaction with dutasteride (CYP3A4 inducers/inhibitors) 6. Patients with cancer or first degree relative with prostate cancer before the age of 50

Design outcomes

Primary

MeasureTime frame
Hair density, Hair diameterTimepoint: 1 month, 3 months, 6 months

Secondary

MeasureTime frame
Number of ADRs assessed by WHO-UMC causality scaleTimepoint: 1 month, 3 months, 6 months

Countries

India

Contacts

Public ContactDr Farida Ahmad

Jawaharlal Nehru Medical College

fahmad32@yahoo.com7417735300

Outcome results

None listed

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