跳至主要内容
临床试验/NCT06845631
NCT06845631招募中不适用

Retrospective-Prospective Clinical Trial Investigating the Treatment of Chronic Pain with the Freedom Peripheral Nerve Stimulation System

Curonix LLC2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年7月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
Curonix LLC
入组人数
40
试验地点
2
主要终点
Pain scores

研究概览

简要总结

This is a retrospective-prospective study in which 40 patients have received a permanent Freedom PNS System. Subjects presented with chronic, intractable pain of peripheral nerve origin refractory to standard medical and/or surgical treatment.

A retrospective chart review will be conducted to assess baseline and follow-up parameters in patients who have received a permanent implant with the Freedom PNS system for at least 12 months. Missing data might be collected after informed consent.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

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

入选标准

  • A. Subject is ≥ 18 years of age at time permanent implant; B. Subject has been implanted with the Freedom PNS system; C. Subject is willing to attend visit as scheduled, and comply with the study requirements (if prospective); D. Patient is capable of giving informed consent.

排除标准

  • A. Subject is currently enrolled in or plans to enroll in any concurrent drug and/or device study while participating in this study (if prospective); B. Any additional active implanted devices for the treatment of chronic pain in addition to the Freedom PNS system.

结局指标

主要结局

Pain scores

时间窗: 12 months

A text description of the subject's pain location(s) and severity will be recorded to correlate with subject feedback. The VRS will be used to measure severity.

次要结局

  • Opioids(12 months)
  • Work status(12 months)
  • GPES(12 months)
  • Amount of sleep(12 months)
  • Sleep disturbances(12 months)
  • EQ-5D-5L(12 months)
  • Claims data(12 months)

研究者

发起方
Curonix LLC
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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