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临床试验/JPRN-jRCT1080224913
JPRN-jRCT1080224913已完成Unknown

Special drug-use survey of Tarlige (evaluation of the efficacy in patients with peripheral neuropathic pain)

DAIICHI SANKYO CO., LTD0 个研究点目标入组 1,890 人开始时间: 2019年10月15日最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
1,890

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 1.Patients with peripheral neuropathic pain not treated with Tarlige tablet before
  • 2.Patients with 12 or more points in the neuropathic pain screening questionnaire
  • 3.Patients with pain lasting more than 3 months
  • 4.Patients with a pain scale of 40 mm or more on VAS before administration of Tarlige tablet
  • 5.Patients who started administration of Tarlige tablet during the contract period (contract period based on the contract with each medical site)
  • 6.Patients who started administration of Tarlige tablet during the registration period
  • 7.Patients from whom written informed consent was obtained

排除标准

  • 1.Patients with a pain scale of 90 mm or less on VAS before administration of Tarlige tablet
  • 2.Patients with other pain unrelated to PNP, that may confound the assessment of PNP
  • 3.Patients with Neurologic disorders (depression, bipolar disorder, schizophrenia, etc.)
  • 4.Patients with dementia, etc. who cannot respond appropriately to questionnaires and VAS for pain

研究者

发起方
DAIICHI SANKYO CO., LTD

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