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临床试验/jRCT2051260093
jRCT2051260093已完成不适用

Double-blind comparative trial of TP-1222

未提供0 个研究点目标入组 360 人开始时间: 待定

试验速览

阶段
不适用
状态
已完成
入组人数
360

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized

入排标准

年龄范围
20age old over 至 No limit(—)
性别
Female

入选标准

  • (1) Age at the time of obtaining informed consent: 20 years or
  • (2) Subjects diagnosed with androgenetic alopecia classified as
  • Ludwig Class I or II.
  • (3) Subjects with disease onset within a specified period
  • (4) Subjects meeting predefined hair criteria required for efficacy

排除标准

  • (1) Subjects with serious comorbidities, or with a history of
  • serious hepatic, renal, cardiac, or hematologic disease.
  • (2) Subjects receiving treatment for hypotension or
  • hypertension.
  • (3) Subjects with concomitant skin diseases at the application
  • site other than androgenetic alopecia.
  • (4) Subjects who have participated in another clinical trial and
  • received an investigational product within 16 weeks prior to the
  • start of investigational product administration in this study.
  • (5) Subjects with alopecia other than androgenetic alopecia.
  • (6) Subjects who have received treatments that may affect hair
  • growth (e.g., minoxidil, hormonal treatments, hair regeneration
  • (7) Pregnant or breastfeeding women

研究者

发起方
未提供

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