TCTR20230916002Enrolling By Invitation3 期
Comparing the Efficacy of Perioperative Pain Control Between Intravenous Parecoxib and Oral Etoricoxib in ACL Reconstruction: A Randomized Controlled Trial
Faculty of Medicine, Prince of Songkla University0 个研究点目标入组 160 人开始时间: 2023年9月16日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 160
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 50 Years(—)
- 性别
- All
入选标准
- •The patients diagnosed as anterior cruciate ligament injury aged 18-50 years old who scheduled for arthroscopic ACLR.
排除标准
- •1. Patient who schedules for bone-patellar tendon-bone autograft ACL reconstruction
- •2. Allergy to acetaminophen, aspirin, sulfonamide, NSAIDs or opioids
- •3. History of dyspepsia, peptic ulcer, or abnormal bleeding
- •4. History of ASCVD (History of diagnosis ACS, clinical likely ACS)
- •5. History of CKD
- •6. History of asthma or COPD because selective COX-inhibitor induce spasm
- •7. History of cerebrovascular disease
- •8. History of peripheral arterial disease
- •9. Patients who have Kratom or Marijuana used or substance abuse
- •10. Patients who anesthesiologist concerns the risk of general anesthesia (GA) is higher than spinal anesthesia; hence, they prefer to use spinal anesthesia rather than general anesthesia
- •11. Pre-operative abnormal EKG or laboratory result e.g., high Cr clearance, abnormal coagulogram
研究者
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