跳至主要内容
临床试验/EUCTR2007-000483-25-IT
EUCTR2007-000483-25-IT进行中(未招募)不适用

Buprenorfina TDS in old patients with chronic pain not give moderated cancer of intensita serious. Study in open, of Phase IV, not controlled, multicentric, spontaneous - Buprenorfina TDS in old patients with chronic pain does not give moderated cancer of intensita from

OSPEDALE ISRAELITICO DI ROMA0 个研究点目标入组 160 人开始时间: 2007年4月3日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
160

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Pazienti of both seies, eta equal or advanced to 65 years. Pazienti in regimen of ordinary stay in hospital, DH or ambulatoriali. Pazienti with chronic pain do not give present cancer from at least 3 months and of intensita from moderated serious to VAS base them. to 5 cm . Pazienti collaborating in a position to supplying the informed consent written.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patologie neurological delirium tremens, endocranica hypertension, diseases convulsive and neuromuscular myasthenia gravis . cardiorespiratory, coagulopatiche, metabolic, hepatic, renal, gastrointestinal, serious and/or scompensate. Patologie neoplastiche Patologie in action. extend, such cutaneous. Alterazioni to prevent the correct application of the doily. Anamnesi positive for alcoholism, abuse of drugs or drug use. Psicosi in acute phase. Corrected inferior MMSE to 14 for eta and scolarita . Pazient of age inferior to the 65 years. Pazienti with ipersensibilita famous to the oppioidi. intolleranti. Pazienti on anamnestica base to the doilies. Pazienti in therapy with IMAO. Pazienti subordinates to acupuncture.

研究者

发起方
OSPEDALE ISRAELITICO DI ROMA

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