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临床试验/NCT01760161
NCT01760161终止不适用

A Randomised, Double-blind Study to Evaluate the Effect of Bilateral Dual Transversus Abdominis Plane Block on Postoperative Pain and Plasma Concentration of Ropivacaine After Robotic Assisted Laparoscopic Surgery

Aalborg University Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2014年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
80
试验地点
1
主要终点
Pain-score on numerical rating scale

研究概览

简要总结

To evaluate the effects of bilateral dual transversus abdominis plane block on postoperative pain after robotic assited laparoskopic surgery and measure the plasma-level of ropivacain after the bilateral dual transversus abdominis plane block.

详细描述

After randomisation patients for robotic assisted laparoscopic surgery will receive bilateral dual transversus abdominis plane block containing either ropivacain or isotonic potassium chloride.

The investigators will record pain-score, opioid-consumption and sensibility on the abdominal wall in the postoperative periode.

Also a blood sample will be taken at 15, 30, 60, 120 and 240 minutes after the block in order to measure the plasma-level of ropivacain after bilateral dual transversus abdominis plane block.

The investigators assume that there will be significant effect on postoperative pain and that the level of plasma-ropivacain will be acceptable.

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

入选标准

  • patients scheduled for robotic assisted laparoscopis surgery
  • acceptance to participate

排除标准

  • allergies to local analgetics
  • daily use of strong opioids

研究组 & 干预措施

Ropivacain

Active Comparator

Ropicacain 3,75 mg/ml 15 ml x 4 when placing the Bilateral Dual Transverus Abdominis Plane block

干预措施: Ropivacaine (Drug)

Isotonic potassium chloride

Placebo Comparator

Isotonic potassium chloride 15 ml x 4 when placing the bilateral dual transverus abdominis plane block.

干预措施: Isotonic potassium chloride (Drug)

结局指标

主要结局

Pain-score on numerical rating scale

时间窗: 4 hours after surgery

次要结局

  • Administration of opioids(The first 24 hours after surgery.)
  • Pain-score on numerical rating scale(24 hours after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nils Bjerregaard

Consultant Anestetist

Aalborg University Hospital

研究点 (1)

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