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
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