跳至主要内容
临床试验/CTRI/2024/03/063477
CTRI/2024/03/063477尚未招募2 期

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 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方

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. 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.

排除标准

  • 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.

研究者

发起方
Dr Sally Rajkumari

相似试验