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临床试验/NCT02251808
NCT02251808招募中不适用

Satisfaction Survey on PINS Stimulator System for Patients With Parkinson's Disease

Beijing Pins Medical Co., Ltd1 个研究点 分布在 1 个国家目标入组 612 人开始时间: 2014年9月最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
612
试验地点
1
主要终点
Patient Satisfaction as Measured by Giving a Form By PINS Medical.

研究概览

简要总结

This study will be done because the investigators would like to evaluate product satisfaction of two PINS products (product A, product B) that are to evaluate the effectiveness of rechargeable and non-rechargeable Deep Brain Stimulation (at baseline visit and at follow-up visit) and by evaluating their responses to the product satisfaction survey that will be given to them by a study coordinator.

详细描述

Other: IPGs products Patients implanted with the rechargeable IPGs and non-rechargeable were followed before and 3 months after DBS surgery and completed a systematic survey of satisfaction with PINS Stimulator System.

研究设计

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

入排标准

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

入选标准

  • Subject is 18 to 80 years of age.
  • Subject has been diagnosed, by a neurologist, with idiopathic Parkinson's disease.
  • The PD patients can recharge the neurostimulator independently, with favourable compliance and commit to cooperate with the clinical trial study,
  • Subjects are PINS neurostimulator users

排除标准

  • Subject were major depression with suicidal thoughts (a score of >25 on the Beck Depression Inventory II,20 with scoresranging from 0 to 63 and higher scores indicating worse functioning), tumor, abnormality in routine liver and renal function, cerebral infarction, hydrocephalus, encephalatrophy, stroke sequela, heart disease, thrombocytopenia, hyperthermalgesia and any medical or psychological problem that would interfere with the conduction of the study protocol.Patients with symptoms of the midline at the state of off medication such as severe language barrier, dysphagia, disequilibrium, slipping-clutch gaitwere excluded. Patients who had undergone other implantation such as cardiac pacemaker, artificial cochlea because of the accompanied diseases such as were excluded. Patients with history of pallidotomy, stereotactic radiofrequency (Gamma Knife) and cell transplantation were also excluded.

结局指标

主要结局

Patient Satisfaction as Measured by Giving a Form By PINS Medical.

时间窗: 3 months after DBS surgery

Of 612 patients implanted with the rechargeable IPGs and non-rechargeable (including 306 PD received rechargeable IPGs, 306 PD received non-rechargeable IPGs) were followed before and 3 months after DBS surgery and completed a systematic survey of satisfaction with PINS Stimulator System.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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