MedPath

To see the efficacy of oral minoxidil versus topical minoxidil in male pattern hair loss.

Phase 3
Conditions
Health Condition 1: L649- Androgenic alopecia, unspecified
Registration Number
CTRI/2024/03/063576
Lead Sponsor
not applicable
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.All males aged 18-45 yrs of age

2. Males with ( Hamilton Norwood Scale II-IV)

Exclusion Criteria

1.Severe hypertension, moderate hypertension on

antihypertensive therapy

2.Cardiovascular dysfunction

3.History of minoxidil hypersensitivity

4.On treatment with formulation of minoxidil, DHT-

blockers or other treatments for AGA in the past 3 months.

5.Psychiatric or scalp disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Clinical photographic assessment and quantitative <br/ ><br>assessment using densitometer will be done. <br/ ><br>2.Hair density calculation will be done in a square inch <br/ ><br>areaTimepoint: every monthly for 6 months
Secondary Outcome Measures
NameTimeMethod
The number of vellus hairs, terminal hairs determined by their thickness in the specific square inch areaTimepoint: every monthly for 6 months
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