NCT01979354Unknown4 期
The Comparison of 0.15 Milligram Spinal Morphine vs.no Treatment for Morphine Requirement After Video-assisted Thoracoscopic Surgery. A Pilot Randomized Control Study
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Total morphine requirement in 48 hours
研究概览
简要总结
Postoperative pain after Video-assisted Thoracoscopic Surgery (VAT) is still debating. Therefore the investigators conduct a study comparing 0.15 mg spinal morphine and control group in term of analgesia.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
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
- •Age 18 year or over
- •Patient ASA physical status I-III.
- •Scheduled for video-assisted thoracoscopic lobectomy or blebectomy with pleurectomy or pleural abrasion
- •Can operate a patient-controlled analgesia (PCA) device.
排除标准
- •Known hypersensitivity to morphine
- •History of bleeding tendency.
- •Known case of infection at the back
- •Patient refuse for spinal anesthesia
- •History of cerebrovascular disease.
- •Need mechanical ventilatory support during postoperative period
研究组 & 干预措施
Spinal morphine
Active Comparator
0.15 mg spinal morphine
干预措施: Spinal morphine (Drug)
结局指标
主要结局
Total morphine requirement in 48 hours
时间窗: 48 hours
次要结局
- Pain(48 hours)
研究者
Sirilak Suksompong
Associate Professor
Mahidol University
研究点 (1)
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