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临床试验/DRKS00011877
DRKS00011877已完成不适用

Survey of a representative sample of patients after topicala) capsaicin 8% therapyb) lidocaine 5% therapyc) botulinum toxin A injection

Berufgenossenschaftliches Universitätsklinikum Bergmannsheil gGmbH, Abteilung für Schmerzmedizin0 个研究点目标入组 224 人开始时间: 2017年5月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
224

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
one 至 one(—)
性别
All

入选标准

  • All patients who a) received at least one treatment with the topical capsaicin 8% (Qutenza ®) in the own clinic since 2010 b) since 2008 received at least one Versatis® therapy in the own clinic c) since 2014 received at least one Botox® injection in the own clinic

排除标准

  • lack of ability to provide information, cognitive limitations

研究者

发起方
Berufgenossenschaftliches Universitätsklinikum Bergmannsheil gGmbH, Abteilung für Schmerzmedizin

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