NCT01082744已完成3 期
Thoracic Paravertebral Block: a Comparative Study of Ropivacaine With Ropivacaine and Sufentanil for Treating Pain After Video-assisted Thoracic Surgery.
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- morphine consumption during the first 48 hours
研究概览
简要总结
The use of paravertebral catheters is a recommended technique to achieve postoperative analgesia after thoracic surgery. To date there is no consensus on which drug regime (local anesthetics with or without opioid) is best. The aim of this prospective clinical trial is to determine wether the use of ropivacaine and sufentanil injected through a thoracic paravertebral catheter results in decreased acute postoperative pain compared with plain ropivacaine in patients after thoracoscopic lung surgery.
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
- •Patient scheduled for planned video-assisted thoracic surgery
- •Patient that consent to participate
- •Planned placement of paravertebral catheter
- •Patient having a medical insurance
排除标准
- •Patient less than 18 years
- •Refusal to participate
- •Known pregnancy
- •Known allergies to local anesthetics, sufentanil and /or to iodinated contrast material
- •Intolerance to sufentanil and/or morphine
- •Chronic consumption of opiates
- •Preoperative chronic pain syndrome
- •Patient having a contraindication to placement of paravertebrtal catheter
研究组 & 干预措施
Continuous paravertebral block with ropivacaine
Active Comparator
干预措施: Ropivacaine (Drug)
Continuous paravertebral block with ropivacaine and sufentanil
Experimental
干预措施: Ropivacaine + Sufentanil (Drug)
结局指标
主要结局
morphine consumption during the first 48 hours
时间窗: 48 hours
次要结局
- Acute pain(48 hours)
- Biological measurements(48 hours)
- Patient satisfaction(48 hours)
- Chronic pain(3 and 6 monthes)
研究者
研究点 (1)
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