跳至主要内容
临床试验/ACTRN12610000094077
ACTRN12610000094077招募中未知

A randomised, double blind, pilot study to evaluate the distribution and duration of the sensory block after a standard and refined ultrasound guided transversus abdominis plane (TAP) block.

Dr Phillip Cowlishaw0 个研究点目标入组 20 人开始时间: 2010年1月27日最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • All participants undergoing lower abdominal surgery through a midline incision at the Mater Hospital who are scheduled to receive a TAP block

排除标准

  • Pre-existing sensory loss/changes on their abdomen
  • Participants who have received central neuraxial anaesthesia
  • Contraindication to TAP block (Participants with a body mass index (BMI) >38, local sepsis, coagulation abnormalities – platelets < 80, international normalised ratio (INR)>1.5, activated thromboplastin time (APTT)>1.5, local anaesthetic allergy, abnormal anatomy)
  • Children and /or young people (age <18)
  • People with an intellectual or mental impairment
  • People whose primary language is other than English
  • Planned surgical infiltration of local anaesthetic or other regional anaesthetic technique

研究者

发起方
Dr Phillip Cowlishaw

相似试验