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临床试验/NCT00793416
NCT00793416撤回4 期

Accuracy of ShuntCheck and MRI in Detection of Shunt Obstruction in Patients Receiving Shunt Patency Test

NeuroDx Development2 个研究点 分布在 1 个国家开始时间: 2008年11月最近更新:
适应症

试验速览

阶段
4 期
状态
撤回
试验地点
2
主要终点
Exploratory Evaluation of the Utility of ShuntCheck in detection of ShuntFlow in patients admitted with potential shunt obstruction

研究概览

简要总结

The purpose of this study is to examine the role of ShuntCheck and MR Imaging in evaluating the presence or absence of Shunt Obstruction in the patients of Hydrocephalus or Idiopathic Intracranial Hypertension (IIH) undergoing radionuclide test for suspected shunt obstruction. This is an exploratory study to determine how a non-invasive device can assist in detection of presence of flow in these patients.

详细描述

This study aims to correlate findings of ShuntCheck and MRI with the Radionuclide patency study. Patients will be enrolled if they have Hydrocephalus or IIH, present with symptoms of shunt obstruction and will need to undergo shunt patency test and an MRI along with standard of care radionuclide study. The ShuntCheck study will be conducted in a clinic, doctor's office or in an emergency room by the treating physician or by trained health care professionals.

Also, patients who are found with shunt obstruction as diagnosed by Radionuclide study will undergo shunt revision and the findings of the study will be correlated with operative findings. Post Shunt replacement patients who also receive adjustable valve will be evaluated with shunt Check, before and after adjustment of valves to detect changes in flow as detected by shunt check.

This is an exploratory study to determine how a non-invasive device can assist in detection of presence of flow in these patients.

Approximately 20 subjects will be enrolled in a single site in this proof of concept, physician sponsored study. An approved, commercial device will be available to the site prior to start of the study.

研究设计

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

入排标准

年龄范围
35 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult Patients > 35 years capable and willing to consent for their participation or consent obtained from a legal guardian.
  • Patients with an indwelling shunt and clinical assessment strongly suggestive of shunt obstruction
  • Patients are candidates for shunt patency procedures in the elective extension

排除标准

  • Patients <35 years of age
  • Patients with symptoms attributable to valve malfunction or shunt infection
  • Patients who need urgent shunt replacement and therefore cannot wait for the SHUNTCHECK evaluation of shunt patency.
  • Patients with edema or wound of skin overlying the shunt tissue.
  • Patients not capable or not willing to consent to participate in the study

结局指标

主要结局

Exploratory Evaluation of the Utility of ShuntCheck in detection of ShuntFlow in patients admitted with potential shunt obstruction

时间窗: Pre and post shunt revision surgery

次要结局

  • To assess any adverse events that arise from conducting ShuntCheck test To assess the cost effectiveness of ShuntCheck screening upon completion of the study(Pre and post shunt revision surgery)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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