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临床试验/NCT03031054
NCT03031054已完成不适用

The Effect of Hyaluronic Acid in Patients With Carpal Tunnel Syndrome

Tri-Service General Hospital3 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2017年3月1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
35
试验地点
3
主要终点
Change from baseline of severity of symptoms and functional status on 2nd week, 1st, 3rd, 6th month and one year after injection

研究概览

简要总结

Carpal tunnel syndrome (CTS) is the most common peripheral entrapment neuropathy with involving compression of the median nerve in the carpal tunnel. Rather than other progressive disease, CTS is characterized by remission and recurrence. The hydrodissection could decrease the entrapment of nerve to restore blood supply. In addition, the hyaluronic acid was proved to decrease adhension of soft tissue and nerve during operation. The investigators design a randomized, double-blind, controlled trial to assess the effect after ultrasound-guided hydrodissection with hyaluronic acid in patients with CTS.

详细描述

After obtaining written informed consent, patients with bilateral CTS will been randomized into intervention and control group. Participants in intervention group received one-dose ultrasound-guided hydrodissection with hyaluronic acid and control side received one-dose ultrasound-guided injection with normal saline. No additional treatment after injection through the study period. The primary outcome is Boston Carpal Tunnel Syndrome Questionnaire (BCTQ) and secondary outcomes include visual analog scale (VAS), cross-sectional area (CSA) of the median nerve, sensory nerve conduction velocity of the median nerve, and finger pinch strength. The evaluation was performed pretreatment as well as on the 2nd week, 1st, 3rd, 6th month and one year after the treatment.

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
Double (Participant, Outcomes Assessor)

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

  • Age between 20-80 year-old.
  • Diagnosis was confirmed using an electrophysiological study

排除标准

  • Coagulopathy
  • Pregnancy
  • Inflammation status
  • Cervical radiculopathy
  • Polyneuropathy, brachial plexopathy
  • Thoracic outlet syndrome
  • Previously undergone wrist surgery or steroid injection for CTS

研究组 & 干预措施

hyaluronic acid hydrodissection

Experimental

Ultrasound-guided hydrodissection with 2.5cc hyaluronic acid between carpal tunnel and median nerve.

干预措施: Sono-guided injection with hyaluronic acid (Procedure)

Normal saline hydrodissection

Active Comparator

Ultrasound-guided hydrodissection with 2.5cc normal saline between carpal tunnel and median nerve.

干预措施: Sono-guided injection with normal saline (Procedure)

结局指标

主要结局

Change from baseline of severity of symptoms and functional status on 2nd week, 1st, 3rd, 6th month and one year after injection

时间窗: Pre-treatment, 2nd week, 1st, 3rd, 6th month and one year

Boston carpal tunnel syndrome questionnaire (BCTQ) is a frequently used patient-based questionnaire for measurement of CTS which encompasses two components. In total, 11 questions and 8 items were evaluated to rate the symptom severity scale (SSS) and functional status scale (FSS), respectively. Both subscales range from 1 to 5 with a higher score indicating a higher degree of disability. The mean of total SSS and FSS divided with each item score were used for further analysis.

次要结局

  • Change from baseline of pain on 2nd week, 1st, 3rd, 6th month and one year after injection(Pre-treatment, 2nd week, 1st, 3rd, 6th month and one year)
  • Change from baseline of cross-sectional area of the median nerve on 2nd week, 1st, 3rd, 6th month and one year after injection(Pre-treatment, 2nd week, 1st, 3rd, 6th month and one year)
  • Change from baseline of finger pinch on 2nd week, 1st, 3rd, 6th month and one year after injection(Pre-treatment, 2nd week, 1st, 3rd, 6th month and one year)
  • Change from baseline of conduction velocity, amplitude of median nerve on 2nd week, 1st, 3rd, 6th month and one year after injection(Pre-treatment, 2nd week, 1st, 3rd, 6th month and one year)

研究者

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

Yung-Tsan Wu

Attending Physician of Department of Physical Medicine and Rehabilitation

Tri-Service General Hospital

研究点 (3)

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