CTIS2024-513796-40-00进行中（未招募）1 期
Postoperative analgesic effect of orally administrated nefopam after a total knee arthroplasty: a randomized controlled trial (NefPO) - 69HCL20_0111
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 46
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
- •Patient over 18., Patient scheduled for primary PTG under spinal anesthesia, in the orthopedics department of the Croix-Rousse hospital., Patient with an American Society of Anesthesiology (ASA) score between I and III., Patient having agreed to take part in the study and having signed the informed consent form., Patient entitled to social security benefits., Patient willing to return for all study visits.
排除标准
- •Any contraindication for nefopam (known hypersensitivity, past medical history of seizures, urinary retention, benign prostate hyperplasia, angle glaucoma, ischemic cardiomyopathy waiting for revascularization, atrial fibrillation), Medical conditions known to influence the pharmacokinetics of nefopam (chronic kidney failure with Glomerular Filtration Rate (GFR) <30mL/min/1,73m2, liver failure, current treatment with rifampicin, carbamazepine, azoles fungicides, macrolides), Current treatment with benzodiazepines, anxiolytics, antidepressants, histamine H1 antagonists, neuroleptics, baclofen, thalidomide, barbiturates, Medical history of gastric or esophageal surgery., Phenylketonuria, Pregnancy or breastfeeding, Past use of oral nefopam
研究者
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