跳至主要内容
临床试验/NCT06188390
NCT06188390招募中不适用

Comparing Efficacy of Hydrodissection With Hyaluronic Acid vs 5% Dextrose for Carpal Tunnel Syndrome: A Randomized Controlled Trial and Ultrasonographic Evaluation of Median Nerve Gliding

Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
2
主要终点
Boston CTS (carpal tunnel syndrome) questionnaire

研究概览

简要总结

Compare the efficacy on carpal tunnel syndrome (CTS) treatment between hydrodissection with hyaluronic acid (HA) vs 5% dextrose

详细描述

Compare the efficacy on carpal tunnel syndrome treatment between hydrodissection with hyaluronic acid vs 5% dextrose through ultrasonographic evaluation.; 2) Evaluate the association of median nerve gliding results between using duplex Doppler ultrasound and B mode video with cross-correlation algorithm.

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
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

Hyaluronic acid and dextrose are both transparent, which is prepare by technician who is not participate in intervention and assessment

入排标准

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

入选标准

  • 20-80 years old patients with carpal tunnel syndrome

排除标准

  • pregnancy, Diabetes, hypothyroidism, uremia, rheumatoid arthritis, coagulopathy, cervical radiculopathy and patients who has ever received surgery for carpal tunnel syndrome or wrist fracture

结局指标

主要结局

Boston CTS (carpal tunnel syndrome) questionnaire

时间窗: before injection , 2 weeks, 3 months and 6 months after injection.

The Boston CTS questionnaire is self-administered and is composed of two parts: the symptom severity scale (11 questions) and the functional status scale (8 questions).A final score is calculated for each scale (the sum of the individual scores divided by the number of items) and ranges from 1 to 5, with a higher score indicating a more severe handicap.

次要结局

  • Ultrasonography (B mode) of median nerve(before injection , 2 weeks, 3 months and 6 months after injection.)
  • Nerve conduction study (NCS) of median nerve(before injection , 3 months and 6 months after injection.)
  • Ultrasonography (duplex Doppler) of median nerve(before injection , 2 weeks, 3 months and 6 months after injection.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验