NL-OMON40725已完成4 期
Pharmacokinetic Profile of Ropivacaïne after Periarticular Local Infiltration Analgesia for Primary Total Knee Arthroplasty - LIAkin
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •- age 50-80 years
- •- ASA physical health classification I * II
- •- Body Mass Index (BMI) < 40
- •- patient planned for a primary unilateral posterior-stabilized tri-compartmental cemented total knee replacement (Genesis II - PS) under unilateral spinal anesthesia with 2 mL hyperbaric bupivacaine 0.5%
- •- scheduled for fast-track protocol TKA
- •- haemoglobin (Hb) concentration * 7.5 mMol/L
- •- written informed consent
排除标准
- •- Placement of a surgical drain
- •- Contra-indications for spinal anesthesia
- •- Known hypersensitivity to amide-type local anesthetics
- •- Hepatic or renal insufficiency
- •- Use of fluvoxamine, ciprofloxacin, ketoconazole, erythromycin, clarithromycin, itraconazole, or rifampicin because of their effect on ropivacaine clearance.
- •- Any other reason which in the opinion of the investigator makes the patient unsuitable for participation in the study
研究者
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