CTRI/2022/03/041364尚未招募4 期
Study Of Efficacy And Safety Of Oral Minoxidil(2.5MG) V/S Oral Finasteride (1MG) in Male Androgenic Alopecia-A Double Blind Study
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Male patient comes with history or clinical findings suggestive of androgenic alopecia.
- •2. Age group more than 18 years of age and less than 50 years of age
- •3. Hamilton grade 2-6
- •4. Have given written consent before investigation and starting the drug.
- •5. Be able and willing and fit , in the view of investigator , to comply all study procedures
排除标准
- •1. Patient who is hypotensive or hypertensive
- •2. Patients with grade 1 or grade 7 alopecia.
- •3. Patient with cardiac diseases (including angina, coronary artery disease, recent or acute myocardial infarction, pericardial effusion)
- •4. Patients with cerebrovascular diseases
- •5. Patients with deranged liver and kidney function.
- •6. Patients allergic to finasteride or minoxidil.
- •7. Patient on any treatment for androgenic alopecia for last 2 months
研究者
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