EUCTR2006-002286-40-NL进行中(未招募)不适用
Chronic Pain Management after HerniorraphyPregabaline versus Placebo
Pfizer bv0 个研究点目标入组 135 人开始时间: 2006年11月24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
- 135
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
- Male
入选标准
- •1.History of unilateral inguinal herniotomy
- •2.Establishment of neuropathic character of chronic pain by means the LANSS painscore and DN4 score
- •3.Abnormal sensitivity (allodynia, dysesthesia, hypoesthesia or dysesthesia) in or around the incisional area
- •4.Duration pain = 3 months
- •5.Gender: Male
- •6.Medial or lateral inguinal hernia
- •7.Age = 18 years
- •8.Description III or IV of pain interfering with daily activity
- •9.VAS score = 40 mm on Vas scale on which they indicate ‘how unpleasant or disturbing the worst pain was that they had today’
- •10.Informed consent (addendum V)
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1.Participation in another trial
- •2.Bilateral hernia
- •3.Recurrent hernia
- •4.Age < 18 years
- •5.Cognitive disfunction
- •6.Patient is unable to speak Dutch
- •7.Description I or II of pain interfering with daily activity
- •8.Patient classified as American Society of Anaesthesiologist Class 4
研究者
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