跳至主要内容
临床试验/NL-OMON24924
NL-OMON24924已完成不适用

Botulinum toxin A in the treatment of orofacial tardive dyskinesias: a single blind study.

Botulinum toxin A ampules by Ipsen, pharmaceutical group0 个研究点目标入组 14 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
14

研究概览

简要总结

Prog Neuropsychopharmacol Biol Psychiatry. 2008 Feb 15;32(2):507-9. Epub 2007 Oct 13.

研究设计

研究类型
Interventional

入排标准

入选标准

  • Patients suffering from orofacial tardive dyskinisias for at least 3 months, stable dosage of psychopharmacological medication and written informed consent by the patient.

排除标准

  • Age younger than 18 years, contraindication for botulinum toxin (myasthenia gravis, Lambert Eaton Myasthenic Syndrome) and women known to be pregnant or having a positive pregnancy test.

研究者

发起方
Botulinum toxin A ampules by Ipsen, pharmaceutical group

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