Opioid Consumption After Orthopaedic Surgery: Prospective Randomized Trial on the Effects of Pre-Operative Counseling
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 237
- 试验地点
- 2
- 主要终点
- Number of pills consumed
研究概览
简要总结
Postoperative pain management and opioid consumption following outpatient orthopaedic surgery may be influenced by a number of variables including knowledge of safe opioid use. A prospective randomized study is designed to understand the effect of preoperative opioid counseling on postoperative opioid consumption and the typical opioid consumption patterns following common outpatient orthopaedic surgeries. The hypothesis was that patients who received preoperative opioid counseling will consume less postoperative opioid medication and experience greater satisfaction with pain management.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients undergoing shoulder, elbow, wrist, knee, foot, and/or ankle surgery
排除标准
- •male of female less than 18 years old
- •patients schedule to undergo inpatient procedures
- •patients undergoing surgeries distal to the wrist
- •patients undergoing surgeries under local anesthesia only
研究组 & 干预措施
Peroperative counseling
干预措施: Preoperative opioid counseling (Other)
No preoperative counseling
结局指标
主要结局
Number of pills consumed
时间窗: Up to 6 weeks
Patients asked to keep daily diary which includes number of pills consumed during the post-operative period
次要结局
- Patient satisfaction with pain management: 5 point Likert Scale(Up to 6 weeks)
- Morphine equivalents (MEQ)(Up to 6 weeks)
- Visual Analog Scale (pain) Pain(Up to 6 weeks)