CTRI/2024/03/063477
Not yet recruiting
Phase 2
Comparative study of efficacy and safety profile of topical minoxidil 5% versus oral minoxidil 2.5 mg in patients with androgenetic alopecia in tertiary care teaching hospital,Haldwani,Uttarakhand. - NI
Dr Sally Rajkumari0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: L649- Androgenic alopecia, unspecified
- Sponsor
- Dr Sally Rajkumari
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients Of either sex with androgenetic alopecia ( Males\- Stage 1 To 4 Of Hamilton\-Norwood Scale; Females\- Stage 1 And 2 Of Ludwig Scale).
- •2\. Age 18 years and above.
- •3\. Patients In good general health with no evidence of systemic illness.
- •4\. Patients who will give written informed consent.
Exclusion Criteria
- •1\. Pregnant And lactating women.
- •2\. Children less than 18 years.
- •3\. Patients with systemic disease( PCOD, cardiac patients, epileptic, cancer,etc.)
- •4\. Patients with active scalp infection, seborrheic dermatitis.
- •5\. Patients with alopecia other than androgenetic alopecia.
- •6\. Patients with history of surgical correction of scalp hair.
- •7\. Drug allergy.
Outcomes
Primary Outcomes
Not specified
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