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临床试验/NCT03525938
NCT03525938Unknown不适用

Transversus Abdominis Plane Block for Chronic Postsurgical Orchalgia: SHAM Controlled, Randomized Trial, Three Months Results

Assiut University2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2018年5月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
70
试验地点
2
主要终点
The change of intensity of pain measured by Visual Analogue Pain (VAS ) score

研究概览

简要总结

the study will evaluate the effect of transversus abdominis plane block (TAP) on chronic post-groin surgeries orchalgia (chronic testicular 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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • The inclusion criteria were patients with chronic scrotal pain (orchialgia) that fulfilled the following criteria:
  • pain intensity ≥ 5 on the visual analog scale (VAS),
  • pain that lasted for more than 3 months after groin surgeries,
  • failed conservative treatment with nonsteroidal anti-inflammatory drugs (NSAIDs)

排除标准

  • The exclusion criteria were:
  • patients with other causes of scrotal pain, e.g., epididymitis, orchitis, and hydrocele,
  • patients complaining of groin infection and coagulopathy,
  • patients suffering from hypertension, ischemic heart disease, or psychiatric disorders

研究组 & 干预措施

TAP group

Active Comparator

干预措施: TAP block (Procedure)

SHAM group

Sham Comparator

干预措施: TAP block (Procedure)

结局指标

主要结局

The change of intensity of pain measured by Visual Analogue Pain (VAS ) score

时间窗: The pain assessment will be done one month, 2 month and 3 month postprocedure.

The Visual Analogue Pain (VAS) scale is a tool for intensity of pain scored from 0 to 10, where 0 = no pain and 10 = the worst pain imaginable

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Diab Fuad Hetta

Assuit university, south egypt cancer institute, anesthesia department

Assiut University

研究点 (2)

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