跳至主要内容
临床试验/CTRI/2009/091/000896
CTRI/2009/091/000896已完成3 期

An Open Label, Randomized, Parallel Group, Prospective, Multicentre Clinical Trial for Evaluation of Efficacy and Safety of Fixed Dose Combination of Minoxidil (5%) + Finasteride (0.1%) Lipid Solution in Comparison with Minoxidil (5%) Solution in Adult Male Patients with Androgenic Alopecia

Intas Pharmaceuticals Limited0 个研究点目标入组 270 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
270

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

  • Inclusion Criteria:
  • (1) Male 18 to 45 years of age, with androgenic alopecia with II to V grade on the modified Norwood Hamilton classification
  • (2) Willingness to maintain the same hair style, approximate length, and hair color throughout the study
  • (3) Subjects willing to provide written informed consent

排除标准

  • (1) Concomitant dermatological disorders on the scalp
  • (2) Serious cardiovascular diseases, renal diseases or hepatic diseases
  • (3) History of drug hypersensitivity, breast disorders or testicular disorders
  • (4) Wearing a wig or under gone surgical treatment for hair loss
  • (5) Shaved scalp or undergoing topical scalp treatment
  • (6) Clinically significant abnormalities on physical examination or laboratory tests
  • (7) History of medication interfering with the study objectives
  • (8) Ongoing use of prohibited medications

研究者

相似试验