Comparison of Procedure (PRP) with Medicine (Topical Minoxidil) in the treatment of hair loss.
- Conditions
- Health Condition 1: L649- Androgenic alopecia, unspecified
- Registration Number
- CTRI/2023/05/053205
- Lead Sponsor
- Dr Sujaya S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
1. Patients with male type-baldness of Hamilton–Norwood scale II–V and female pattern baldness of Ludwig scale II-III.
2. Within the age group of 18–60 years.
3. Not using topical minoxidil and oral/topical finasteride for at least 6 months before the start of study
4. Patients providing consent.
1. Patients with inflammation or erythema (except mild seborrheic dermatitis), or scarring over the scalp.
2. Patients on anticoagulants, antihypertensives, anticonvulsants, aspirin, or other nonsteroidal anti-inflammatory drugs.
3. Patients with previous history or current malignancies, platelet or bleeding disorders, bone marrow aplasia, diabetes, HIV, hepatitis B or C infection or immunocompromised patients, and those having a propensity for keloids.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method