EUCTR2011-000506-21-GB进行中（未招募）1 期
A double-blind, randomised placebo-controlled trial to determine whether low-dose intravenous ketamine peri-operatively can prevent chronic post-surgical pain, in patients undergoing thoracotomy or video assisted thoracic surgery (VATS). - RCT of ketamine versus placebo after thoracotomy or VATS surgery (1)
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 104
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
入选标准
- •1. All adult patients (> 18 years) who are undergoing either thoracotomy or VATS. 2. Participants must be able to understand English.
- •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. Patient refusal 2. History of previous chronic thoracic pain 3. Neuropathic pain (whatever the site), existing at time of recruitment 4. Pre-operative analgesic treatments which include the following medications: strong opioids (step 3 analgesics), tricyclic antidepressants, venlafaxine, gabapentin, pregabalin, duloxetine, clonazepam or carbamazepine. 5. Allergy to bupivacaine, morphine, paracetamol, tramadol, dihydrocodeine or ketamine.
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