EUCTR2010-020042-94-AT进行中（未招募）1 期
The Effect of High-dose Remifentanil on the Reversal of Neuropathic Pain in Postherpetic Patients - RemiHighDose PHZ
Medizinische Universität Wien, Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin0 个研究点目标入组 21 人开始时间: 2010年7月27日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 21
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
- •Patients suffering from PHN.
- •Pain = 4 out of 10 in numeric rating scale (NRS)
- •Female and male patients above the age of 18
- •Ability to understand/write/read german
- •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
- •Any of the following will exclude a subject from the study:
- •Zoster affecting trigeminal-, opticus region
- •Any somatic pain which is stronger than the neuropathic pain
- •Severe progressive disease
- •Acute cardiac decompensation
- •Known cardiac valve dysfunction
- •Known pulmonary hypertension
- •Cardiac conduction disturbance
- •Active herpetic lesion
- •Analgesic or antitussive opioid therapy
- •Bronchial asthmal
- •Known chronic obstructive pulmonary disease (COPD) >GOLD II
- •Severe psychiatric condition
- •Abuse of alcoholic beverages, drug abuse
- •Negative neuropathic symptoms
- •Pregnancy or breast feeding
- •Participation in a clinical trial in the 2 weeks preceding the study
- •Allergy against any medication used in the study protocol
研究者
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