TCTR20230428001进行中（未招募）4 期
A prospective, double-blinded, randomized controlled trial to evaluate the efficacy of intravenous nefopam on postoperative opioid consumption after laparoscopic liver surgery
适应症
试验速览
- 阶段
- 4 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
入排标准
- 年龄范围
- 18 Years 至 65 Years（—）
- 性别
- All
入选标准
- •1. Age 18-65 years old
- •2. Patient who undergoing laparoscopic liver surgery
- •3. ASA classification I-III
排除标准
- •1. Severe systemic medical condition such as poor-controlled hypertension, heart disease, lung disease, renal dysfunction with GFR less than 60, poor-controlled diabetes mellitus, Child-Pugh class B or C, Abnormal liver function test (total bilirubin > 2 mg/dL, INR > 1.7, albumin < 3,5 g/dL, or aspartate or alanine aminotransferase > 2 times of upper limit of normal), neuromuscular disease
- •2. Chronic pain problem
- •3. Prescribed analgesic drugs
- •4. Contraindication to nefopam such as tachyarrhythmia, pregnancy, convulsive disorder, taking monoamine oxidase inhibitors
- •5. Allergic to study drugs
- •6. Unable or refusal to use IV PCA
- •7. Unable to understand and report numeric rating pain score
- •8. Anesthetic care personnel plan to do neuraxial or trunk blocks
研究者
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