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Carpal Tunnel Release Using Ultrasound (CiTRUS)

2022年8月16日 更新者:Sonex Health, Inc.

Carpal Tunnel Release Using Ultrasound Patient Experience Registry

The goal of the Carpal Tunnel Release Using Ultrasound registry (CiTRUS Registry) is to collect experience information from patients scheduled to undergo carpal tunnel release surgery with either the SX-One MicroKnife® with ultrasound guidance or the traditional mini-open technique without US guidance.

研究概览

详细说明

The CiTRUS registry is an observational study designed to better understand the overall patient experience following a carpal tunnel release surgery using either the SX-One MicroKnife with ultrasound guidance or the traditional mini-open technique without ultrasound guidance. The determination of which surgical technique to uses will be determined by the treating physician and the patient. The patient registry outcomes are intended to help direct future clinical care, educate patients with carpal tunnel syndrome, and design future research.

研究类型

观察性的

注册 (实际的)

411

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Minnesota
      • Eagan、Minnesota、美国、55121
        • Sonex Health, Inc.

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Patients scheduled to undergo carpal tunnel release surgery using either the SX-One MicroKnife® with ultrasound (US) guidance or the traditional mini-open technique without ultrasound guidance.

描述

Inclusion Criteria:

  • Scheduled to undergo carpal tunnel release surgery on the right and/or left wrist using either the SX-One MicroKnife with US guidance or the traditional mini-open technique without US guidance
  • 18 years of age or older
  • Agree to complete questionnaires over a 12-month period
  • Valid mobile phone number and email address to receive and answer questions

Exclusion Criteria:

• Age less than 18 years

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
SX-One MicroKnife with ultrasound guidance
Carpal Tunnel Release using the SX-One MicroKnife with ultrasound guidance
Carpal Tunnel Release surgery involves transecting the transverse carpal ligament (TCL) in order to reduce median nerve compression and alleviate symptoms. The carpal tunnel release surgery will be performed using the SX-One MicroKnife with ultrasound guidance.
Carpal Tunnel Release surgery involves transecting the transverse carpal ligament (TCL) in order to reduce median nerve compression and alleviate symptoms. The carpal tunnel release surgery will be performed using the traditional mini-open technique without ultrasound guidance.
Traditional mini-open technique without ultrasound guidance
Carpal Tunnel Release using the traditional mini-open technique without ultrasound guidance
Carpal Tunnel Release surgery involves transecting the transverse carpal ligament (TCL) in order to reduce median nerve compression and alleviate symptoms. The carpal tunnel release surgery will be performed using the SX-One MicroKnife with ultrasound guidance.
Carpal Tunnel Release surgery involves transecting the transverse carpal ligament (TCL) in order to reduce median nerve compression and alleviate symptoms. The carpal tunnel release surgery will be performed using the traditional mini-open technique without ultrasound guidance.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change from baseline Quick Form of the Disabilities of the Shoulder and Hand scores at 12 months
大体时间:12 months
To assess the overall patient experience following carpal tunnel release using either the SX-One MicroKnife® with ultrasound (US) guidance or the traditional mini-open technique without ultrasound guidance patients will complete the Quick Form of the Disabilities of the Shoulder and Hand scale. The Quick Form of the Disabilities of the Shoulder and Hand scale consists of 11 items scored 1-5 with lower scores indicating less symptoms or better function.
12 months
Change from baseline Boston Carpal Tunnel Questionnaire scores at 12 months
大体时间:12 months
To assess the overall patient experience following carpal tunnel release using either the SX-One MicroKnife® with ultrasound guidance or the traditional mini-open technique without ultrasound guidance patients will complete the Boston Carpal Tunnel Questionnaire at 12 months. The Boston Carpal Tunnel Questionnaire consists of two subscales: symptom severity (11 items scored 1-5) and functional status (8 items scored 1-5) with lower scores indicating less symptoms or better function.
12 months

次要结果测量

结果测量
措施说明
大体时间
Patient reported time to return to activities
大体时间:Post-operative days 1-14, 2 weeks, 1,3,6 and 12 months
Patient reported time to return to normal activities as measured in days.
Post-operative days 1-14, 2 weeks, 1,3,6 and 12 months

其他结果措施

结果测量
措施说明
大体时间
Patient reported satisfaction following carpal tunnel release
大体时间:2 weeks, 1,3,6 and 12 months
Patient reported satisfaction with the carpal tunnel release procedure on a 1-5 scale with higher numbers indicating greater satisfaction.
2 weeks, 1,3,6 and 12 months
Patient reported symptom improvement following carpal tunnel release
大体时间:2 weeks, 1,3,6 and 12 months
Patient reported improvement in symptoms following carpal tunnel release, reported on a 1-5 scale with higher numbers indicating more symptom improvement.
2 weeks, 1,3,6 and 12 months
Pain reported pain on numerical pain rating scale
大体时间:Post-operative days 1-14, 2 weeks, 1,3,6 and 12 months
Patient reported pain following carpal tunnel release, reported on an 11-point (0-10) numerical pain rating scale with higher numbers indicating more pain.
Post-operative days 1-14, 2 weeks, 1,3,6 and 12 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Jay Smith, MD、Sonex Health, Inc.

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年7月2日

初级完成 (实际的)

2022年8月1日

研究完成 (实际的)

2022年8月15日

研究注册日期

首次提交

2021年8月26日

首先提交符合 QC 标准的

2021年8月26日

首次发布 (实际的)

2021年9月1日

研究记录更新

最后更新发布 (实际的)

2022年8月18日

上次提交的符合 QC 标准的更新

2022年8月16日

最后验证

2022年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

是的

在美国制造并从美国出口的产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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