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临床试验/NCT05348330
NCT05348330已完成不适用

Mid-point to Pleura Transverse Process Continuous Block Versus Thoracic Intervertebral Foramen Continuous Block, for Analgesia in Polytraumatic Patients with Multiple Rib Fractures

San Salvatore Hospital of L'Aquila2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年12月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
Pain intensity

研究概览

简要总结

The analgesic effect of continuous mid-point to pleura transverse process block compared to the analgesic effect of continuous thoracic intervertebral foramen block, in patients with multiple rib fractures.

详细描述

The analgesic effect of continuous mid-point to pleura transverse process block will be compared to the analgesic effect of continuous thoracic intervertebral foramen block, in patients with multiple rib fractures, by using the numeric rating scale (NRS) for pain.

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ribs fracture after polytrauma

排除标准

  • pregnancy
  • allergy to anesthetics
  • head trauma
  • history of neurological impairment (primary or secondary)
  • history of cancer
  • history of chronic obstructive pulmonary disease
  • infections of skin close to the block site
  • systemic infections

结局指标

主要结局

Pain intensity

时间窗: First 72 hours from the block

The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable"

次要结局

  • Sensory block(First 72 hours from the block)
  • Blood pressure(First 72 hours from the block)
  • Request of analgesic drugs(First 72 hours from the block)
  • Anesthetic spread(First 72 hours from the block)
  • Complication(First 72 hours from the block)
  • Arterial blood gas analysis(First 72 hours from the block)
  • Airflow rate(First 72 hours from the block)
  • Diaphragmatic motion(First 72 hours from the block)

研究者

发起方
San Salvatore Hospital of L'Aquila
申办方类型
Other
责任方
Principal Investigator
主要研究者

Emiliano Petrucci

Medical Doctor

San Salvatore Hospital of L'Aquila

研究点 (2)

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