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临床试验/NCT04737239
NCT04737239已完成不适用

Corticosteroid Injection Effectiveness in Carpel Tunnel Patients With Negative or Mild EMG

Henry Ford Health System1 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2020年12月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
61
试验地点
1
主要终点
Boston Carpel Tunnel Questionnaire

研究概览

简要总结

Carpal Tunnel Syndrome (CTS) is the most common nerve entrapment syndrome worldwide. There are currently no studies examining the effectiveness of corticosteroid injections in patients with normal (negative) EMG studies. The purpose of this study is to gain a better understanding of the duration of symptom improvement post corticosteroid injection in patients with negative or mild EMG studies. The Boston Carpal Tunnel Questionnaire will be given to patients undergoing corticosteroid injections for the treatment of carpal tunnel syndrome to assess their response to the injection. Investigators will collect data retrospectively. The Boston Carpal Tunnel Questionnaire (BCTQ) is administered as per standard protocol to all patients with CTS who have a negative or mild EMG study. The BCTQ assesses the patient's self-reported symptom severity and functional status. Investigators will analyze this data with respect to demographics as well as numbness in the median n. distribution, nocturnal numbness, weakness/atrophy of the thenar musculature, Tinel's sign, Phalen's test, loss of 2-point discrimination, Quick-Dash score, and grip strength score.

The primary outcome will be the Boston Carpal Tunnel Questionnaire outcome score under the different EMG conditions.The secondary outcomes will be numbness in the median n. distribution, nocturnal numbness, weakness/atrophy of the thenar musculature, Tinel's sign, Phalen's test, loss of 2-point discrimination, QuickDash score, and grip strength score. Both outcomes will be examined in patients with negative or mild EMG readings. This information will allow orthopedic physicians to gain a better understanding of the duration of symptom improvement post-corticosteroid injection, allowing them to fine tune their treatment plans for CTS patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients who speak English
  • •Patients who are 18 years or older
  • •Patients who are clinically diagnosed with CTS
  • •Patients who have a negative or mild EMG study
  • •Patients who receive a corticosteroid injection after obtaining a negative or mild EMG study

排除标准

  • •Patients who do not speak English
  • •Patients who are younger than 18 years of age
  • •Patients who have experienced previous trauma to the wrist
  • •Patients who have had previous treatment for CTS including but not limited to corticosteroid injection or surgery
  • •Patients with a moderate or severe EMG study

研究组 & 干预措施

Patient with CTS/Mild EMG

干预措施: Corticosteroid injections for CTS treatment (Other)

Patient with CTS/Negative EMG

干预措施: Corticosteroid injections for CTS treatment (Other)

结局指标

主要结局

Boston Carpel Tunnel Questionnaire

时间窗: Dec 23 2020-Dec 22 2021

Scaled 1-5, higher scores indicate worse outcomes

次要结局

  • Number of patients with positive Phalen's Test(Dec 23 2020-Dec 22 2021)
  • Number of patients with numbness in the median n. distribution(Dec 23 2020-Dec 22 2021)
  • Number of patients with weakness/atrophy of the thenar musculature(Dec 23 2020-Dec 22 2021)
  • Number of patients with positive Tinel's Sign(Dec 23 2020-Dec 22 2021)
  • QuickDash score(Dec 23 2020-Dec 22 2021)
  • Grip Strength score(Dec 23 2020-Dec 22 2021)
  • 2-point discrimination Test(Dec 23 2020-Dec 22 2021)

研究者

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

Charles S Day

Orthopedic Surgeon

Henry Ford Health System

研究点 (1)

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