CTIS2024-511010-21-00进行中（未招募）1 期
(PREVENT)A Randomized, Double-blind, Placebo-controlled Trial on the Prevention of Chronic Postoperative Pain after Inguinal Hernia and Knee Surgery by Postoperative Treatment with Tapentadol
eids Universitair Medisch Centrum (LUMC)0 个研究点目标入组 540 人开始时间: 2024年7月9日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 540
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 65+（—）
- 性别
- All
入选标准
- •American Society of Anesthesiologists score 1, 2 or 3, Age between 18-80 years
排除标准
- •Chronic pain due to any cause other than pain caused by osteoarthritis of the knee or inguinal hernia which in the opinion of the investigator may influence the outcome of the trial;, Regular use of anti-depressants or anti-epileptics for chronic pain. If this medica-tion is used for another indication than pain participation in the study is allowed., Known allergies or contraindication to the study medication according to the SmPC (such as the presence of respiratory depression, severe astma, paralytic ileus and acute intoxications with alcohol, hypnotics or other psychotropic active substances);, Pregnancy/lactation;, Use of MAO-inhibitors or rifampicin within the last 14 days before inclusion;, Inability to perform psychophysical testing (eg. in case of cognitive or psychiatric disorders, Inability to give informed consent, Inability to communicate with the investigators
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