NCT02440542撤回不适用
Popliteal Nerve Block for Postoperative Pain Control in Patients Undergoing Ankle and Hindfoot Reconstruction About the Talus
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 主要终点
- Pain rating
研究概览
简要总结
The purpose of this study is to evaluate outcomes of popliteal nerve blocks for postoperative pain control in patients undergoing ankle and hindfoot reconstruction surgeries. The following outcomes will be analyzed: length of hospital stay, level of pain control, pain medication use, complications, and patient satisfaction.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
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
- •Adult patients ≥ 18 years old
- •Patients undergoing ankle, subtalar, pantalar, triple, or tibiotalocalcaneal arthrodesis (CPT codes 27870, 28715, 28725, or 28740)
- •Patients undergoing total ankle arthroplasty (CPT code 27702)
- •Patients with a preoperative surgical plan to receive a popliteal nerve block during the postoperative period
- •Patients whom can be reasonably expected to understand and comply with patient-reported postoperative data collection and surveys
排除标准
- •Patients undergoing an ankle or hindfoot reconstruction procedure whom are medically ineligible to receive a safe popliteal nerve block (i.e. patients with neuropathy)
- •Patients with documented substance abuse (i.e. history of narcotic abuse could confound pain outcomes)
结局指标
主要结局
Pain rating
时间窗: Postoperative- through 12 weeks
Measured by VAS
次要结局
- Narcotic intake(Postoperative- through 12 weeks)
- Hospital length of stay(Postoperative- through day of hospital discharge (discharge same day of surgery to approximately 3 days postop))
- Patient satisfaction(Postoperative- through first surgical follow-up (up to 3 weeks))
研究者
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