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临床试验/NCT03968523
NCT03968523已完成不适用

Loco/Regional Anaesthesia Evaluation in Laparoscopic Hernioplasty

Hospital Italiano de Buenos Aires2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2019年4月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
62
试验地点
2
主要终点
Postoperative pain

研究概览

简要总结

Laparoscopic hernioplasty is associated with lesser postoperative pain and quick return to work. TAP block is the gold standard technique in this type of hernioplasty. Our aim is to compare TAP block with a novel local infiltration technique that uses direct laparoscopical vision.

详细描述

Laparoscopic hernioplasty is associated with lesser postoperative pain and quick return to work. TAP block is the gold standard technique in this type of hernioplasty. Our aim is to compare TAP block with a novel local infiltration technique that uses direct laparoscopical vision. Patients will be randomized into two arms of intervention that will be compared by a blind analysis. Primary outcomes will be postoperative pain evaluated systematically until 30 days postoperative, and analgesic consumption.

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)

盲法说明

Each patient will be included in one cohort of treatment by a randomized criteria.

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

  • 18 years or more.
  • Programmed inguinal laparoscopic hernioplasty

排除标准

  • Allergic to medication prescribed
  • Story of mesh rejection

结局指标

主要结局

Postoperative pain

时间窗: 30 days postoperative

Postoperative main measured by an visual analogue scale

次要结局

  • Analgesics consumption(30 days postoperative)
  • type of analgesic consumption(30 days)
  • pain at the moment of need of analgesics take(30 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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