NCT01825993Unknown3 期
RANDOMISED STUDY ABOUT POTSOTERATORY PAIN CONTROL IN LAPAROSCOPIC SIGMOIDECTOMY
Corporacion Parc Tauli1 个研究点 分布在 1 个国家目标入组 225 人开始时间: 2013年4月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 发起方
- 入组人数
- 225
- 试验地点
- 1
- 主要终点
- EVA (POSTOPERATIVE PAIN)
研究概览
简要总结
The investigators would study the control of postoperative pain with peridural catheter, morphine PCA ev or Transabdominal block.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age more than 18
- •Laparoscopic sigmoidectomy
- •Informed consent firmed
排除标准
- •Urgent surgery
- •Sigmoid tumour stage IV
- •Cronic pain treatment
- •No informed consent firmed
- •Paliative surgery
研究组 & 干预措施
PCA endovenous
Experimental
1mg/10 min Morphine
干预措施: MORPHINE (Drug)
PERIDURAL CATHETER
Active Comparator
Peridural L-bupivacaine 0.25%
干预措施: L-BUPIVACAINE ; MORPHINE (Drug)
TANSABDOMINAL BLOCK (TAP)
Active Comparator
L-BUPIVACAINE im
干预措施: L-BUPIVACAINE ; MORPHINE (Drug)
结局指标
主要结局
EVA (POSTOPERATIVE PAIN)
时间窗: 72 H POSTOPERATIVE
The investigators asked the patient the postoperative pain during teh first 72 hours by EVA scale.
次要结局
- ADVERSE EFFECTS(five days)
研究者
LAURA MORA LOPEZ
General Surgeon
Corporacion Parc Tauli
研究点 (1)
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