跳至主要内容
临床试验/EUCTR2013-000521-31-ES
EUCTR2013-000521-31-ES进行中(未招募)1 期

Efficacy and safety of gabapentin versus placebo to prevent the incidence of PostHerpetic Neuralgia

Gerencia de Atención Primaria de Mallorca0 个研究点开始时间: 2013年10月22日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方

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

  • Patient aged >= 50 , diagnosed by uncomplicated herpes zoster with a < de 72h onset.
  • Visual analog scale of pain ? 4 (rated 0 to 10).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 54
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 80

排除标准

  • Current or anticipated treatment with gabapentine or triciclys antidepresants
  • Patients diagnosed of hepatic insufficiency
  • Patients with a a history of intolerance of hipersensitivity to gabapentin or excipients.
  • Patients with impaired renal function (Clcr <79ml/min)
  • Patients with evidence of cutaneous, ocular or visceral disemination of herpes zoster infection (cutaneous disemination is defined as > 20 discrete lesion outside adjacent dermatomes) evidencia de diseminación cutánea o visceral del HZ (más de 20 lesiones fuera del
  • dermatoma adyacente)
  • Patients who have received inmunosupresive therapy in the last 3 months or inmunomodulatory medication (including interferon) within the previous 4 weeks
  • Patient diagnosed of inmunodeficiency

研究者

发起方
Gerencia de Atención Primaria de Mallorca

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