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临床试验/JPRN-UMIN000000474
JPRN-UMIN000000474已完成2 期

Double-blind Placebo-controlled Clinical Trial of Leuprorelin acetate in Patients with Spinal and Bulbar Muscular Atrophy (SBMA) - Clinical Trial of Leuprorelin acetate in Patients with SBMA

Department of Neurology, Nagoya University School of Medicine0 个研究点目标入组 40 人开始时间: 2006年9月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40

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
30years-old 至 70years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1) Patients with past medical history of allergy to leuprorelin acetate 2) Patients who have severe complications and are not appropriate to participate to the trial.. 3) Patients who have taken testosterone within 8 weeks prior to the informed consent.

研究者

发起方
Department of Neurology, Nagoya University School of Medicine

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