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临床试验/ISRCTN59894749
ISRCTN59894749已完成未知

Injection or Decompression in Carpal Tunnel Syndrome - Pilot Study (INDICATE­-P)

Gloucestershire Hospitals NHS Foundation Trust0 个研究点目标入组 40 人开始时间: 2016年7月20日最近更新:
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适应症

试验速览

阶段
未知
状态
已完成
入组人数
40
研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

2017 protocol in https://www.ncbi.nlm.nih.gov/pubmed/28451442 2020 letter in https://pubmed.ncbi.nlm.nih.gov/32501127/ (added 22/04/2021)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • •1. All three of the following must be present:
  • •1.1. Intermittent paraesthesia in median nerve distribution
  • •1.2. Nocturnal hypoaesthesia, dysaesthesia or paraesthesia (including on waking)
  • •1.3. A positive provocation test (e.g. Tinel’s, Phalen’s, Durkin’s pressure or hand elevation test)
  • •2. Symptoms present for at least 3 months
  • •3. Patients’ symptoms must either:
  • •3.1. Disturb their sleep
  • •3.2. Limit their ability to perform work or activities of daily living
  • •4. Patients must have failed a trial of night splints for at least 2 weeks
  • •5. Age >18 years

排除标准

  • •1. Severe CTS
  • •1.1. Thenar muscle wasting or
  • •1.2. Continuously reduced light touch sensation in median nerve distribution (compared to opposite unaffected side or unaffected finger)
  • •2. Previous carpal tunnel surgery or steroid injection (either side)
  • •3. CTS secondary to:
  • •3.1. Wrist deformity, trauma or mass
  • •3.2. Pregnancy
  • •3.3. Hypothyroidism
  • •3.4. Inflammatory arthropathy
  • •4. Clinical or neurophysiological evidence of polyneuropathy or cervical radiculopathy
  • •5. Other symptomatic disorder in the affected hand diagnosed in the last 6 months or requiring treatment.
  • •6. Patients in whom the baseline questionnaire cannot be completed due to cognitive difficulties

研究者

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