A clinical trial to study the effect of topical minoxidil 5% solution alone and a combination topical minoxidil 5% and finasteride 0.1% solution for the treatment of common baldness in me
Phase 4
- Conditions
- Health Condition 1: null- Male pattern hair loss
- Registration Number
- CTRI/2017/10/010054
- Lead Sponsor
- Government Medical College and Hospital Sector Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients with clinical diagnosis of male pattern baldness with Modified Norwood-Hamilton grading III vertex, IV and V
2. Duration of hair loss less than 5 years
Exclusion Criteria
1. Any systemic or topical treatment for hair loss in last 6 months
2. Any significant cardiovascular diseases like coronary artery disease, congestive heart failure, cardiac dysrhythmias or valvular disease
3. Unrealistic expectations
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The three primary efficacy and safety outcome measures will be the change in total and terminal hair count, scoring of the global photographs by blinded evaluators and adverse events, assessed in both the groups <br/ ><br>Timepoint: 12 weekly <br/ ><br>
- Secondary Outcome Measures
Name Time Method The secondary efficacy outcome measure will be the patients subjective hair growth assessment score.Timepoint: 12 weekly