NCT02196727已完成不适用
Evaluation of Post-operative Pain in Bascom Cleft Lift Operation Receiving Multimodal Analgesia and Spinal Saddle Block in Day Case Surgery Setting.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- Numerical Rating Scale (NRS) pain score (0=no pain, 10= maximum imaginable pain)
研究概览
简要总结
The purpose of this study is to evaluate postoperative pain in Bascom Cleft Lift operation receiving multimodal analgesia in day-case surgery setting.
Hypothesis: Multimodal analgesia provides adequate pain relief in patients undergoing Bascom Cleft Lift operation.
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 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age > 18
- •ASA physical status 1 and 2
- •Patient undergoing Bascom operation in prone position
排除标准
- •Pregnancy
- •Current regular use of drug belonging to the class of opioids
- •Allergy/ intolerance to drugs included in multimodal analgesia regime
结局指标
主要结局
Numerical Rating Scale (NRS) pain score (0=no pain, 10= maximum imaginable pain)
时间窗: 24 hours postoperatively
次要结局
- Numerical Rating Scale (NRS) pain score (0=no pain, 10= maximum imaginable pain)(2 hours, 48 hours and 30 days postoperatively)
研究者
Saphana Jassim Mohamed
Consultant
Hvidovre University Hospital
研究点 (1)
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