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临床试验/ACTRN12612000537853
ACTRN12612000537853尚未招募未知

Comparing the pain of injection of a single injection palmar subcutaneous nerve block with a double injection dorsal digital nerve block for digital anaesthesia in patients who present to the emergency department with finger injuries.

Royal Brisbane and Womens Hospital0 个研究点目标入组 90 人开始时间: 2012年5月21日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
90

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

  • Patients will be included if they
  • 1. are aged >= 18 years old and
  • 2. present with a finger injury requiring digital anaesthesia

排除标准

  • Patients will be excluded if they:
  • 1. Have a digital nerve injury proximal to distal interphalangeal joint. Such patients are excluded because assessment of the distal sensation of the finger is performed by the hand surgical team as these injuries benefit from operative intervention.
  • 2. Have peripheral neuropathy or vasculopathy. Peripheral neuropathy will confound the assessment of pain of the injection and all pain scores. Vasculopathy will result in reduced blood flow to the digit and may result in increased risk vascular compromise following digital anaesthesia.
  • 3. Are unwilling or unable to consent. This includes patients with a psychotic illness that would impair their ability to consent and patients with alcohol or drug intoxication.
  • 4. Have a tendon sheath infection as digital nerve block may promote the spread of the infection
  • 5. Skin disease such as eczema overlying the injection site
  • 6. Have an allergy to lignocaine

研究者

发起方
Royal Brisbane and Womens Hospital

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