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临床试验/NCT03345511
NCT03345511已完成不适用

Ultrasound Guided Analgesic Caudal Block in Anal Canal Surgery

Universidad de Antioquia1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2015年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
23
试验地点
1
主要终点
postoperative pain intensity (P3). Self reported pain intensity at 6, 12 and 24 hours after surgery.

研究概览

简要总结

Interventional study that evaluate analgesia and side effects of Ultrasound guided Caudal block preoperatively in benign canal anal surgery

详细描述

Postoperative pain is an important symptom in patients after benign anal canal surgery. Caudal block has been described to decrease postoperative pain in this type of surgery. Ultrasound is a tool that facilitates its performance and increases the rate of a successful block.

Objective

To determine the usefulness of ultrasound guided caudal block in anesthesia and postoperative analgesia in patients scheduled for benign anal surgery. Methods : Interventional study in adult patients that received ultrasound caudal anesthetic block before benign anal surgery. The investigators evaluated analgesic efficacy of this intervention by mean of numeric rating scale ( NRS) for pain after 6, 12 and 24 hours of surgery, rescue analgesia, motor block, urinary retention, surgical conditions and patient satisfaction in postoperative period.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age from 18 to 70 year old patient
  • schedule for benign anal surgery ( hemorrhoids, anal fistula, fissure or abcess )
  • Caudal analgesic injection before surgery
  • Use of ultrasound to guide needle insertion into caudal space

排除标准

  • cognitive impairment
  • verbal communication impairment
  • infection in skin at injection site
  • coagulopathy
  • technique refusal

研究组 & 干预措施

Ultrasound Guided Caudal Block

Experimental

30 minutes before benign canal anal surgery, a 18 G tuohy needle guided with an ultrasound probe to visualize the caudal space, a solution of bupivacaine 0.25%, Lidocaine 1% and dexamethasone 8mg was injected and needle removed.

干预措施: Ultrasound Guided Caudal Block (Procedure)

结局指标

主要结局

postoperative pain intensity (P3). Self reported pain intensity at 6, 12 and 24 hours after surgery.

时间窗: 1 day

The pain numeric Rating Scale (NRS) is a single 11-point numeric scale in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of their pain , with 0 representing one pain extreme (e.g., "no pain") and 10 representing the other pain extreme (e.g., "pain as bad as you can imagine" and "worst pain imaginable")

次要结局

  • Rescue Analgesia (R3) need of opioid medication for rescue severe postoperative pain at 6, 12 and 24 hours after surgery.(1 day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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