跳至主要内容
临床试验/IRCT20210823052264N7
IRCT20210823052264N7招募中3 期

Efficacy of low dose oral minoxidil Versus topical minoxidil solution for the treatment of androgenetic alopecia.

Combined Military Hospital Quetta0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
80

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

年龄范围
18 years 至 55 years(—)
性别
Male

入选标准

  • Clinical diagnosis of AGA score 2-5 on Norwood-Hamilton classification.
  • Age between 18-55 years.
  • Patients who haven't received topical or systemic treatment for AGA within 3 months prior to the study.

排除标准

  • Those with other causes of hair loss Such as inflammatory or scarring alopecia.any other types of alopecia
  • History of severe systemic diseases ( renal, cardiovascular and hepatic)
  • History of some hormonal disorders.
  • History of hypertension,hypotension or on any antihypertensive therapy
  • Hypersensitivity to minoxidil.

研究者

发起方
Combined Military Hospital Quetta

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