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临床试验/NCT03113799
NCT03113799已完成不适用

A Study to Evaluate the Performance and Safety of Aqueduct's Smart External Device (SED) Compared to Standard EVD Drains

Aqueduct Critical Care4 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2017年4月12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
发起方
入组人数
56
试验地点
4
主要终点
Staff interactions

研究概览

简要总结

To evaluate the performance characteristics of the Smart External Drain (SED) compared with standard EVD drains in the hospital setting, specifically:

  • Number, type and duration of staff interactions.
  • Regulating and controlling ICP and CSF drainage.
  • Maintaining system control with patient movement.

详细描述

In this two day clinical trial, subjects will be observed on Day 1 of study during their routine treatment and using their already existing EVD. On Day 2 of study; subjects will be switched to the Smart External Drain for monitoring and management of ICP and CSF

研究设计

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

入排标准

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

入选标准

  • Stable Neuro - examination on standard EVD assessed as Not Clinically Significant (NCS) by PI or delegated Sub-I prior to study treatment.
  • GCS > 13 (minimum of E3V5M5) prior to study treatment.
  • Subject must be scheduled to have an EVD placed as part of routine management and for a length of at least 48 hours. (e.g. in the setting of a tumor removal or treatment of hydrocephalus)
  • Stable Vital Signs - Blood pressure (Systolic and Diastolic), Heart Rate, Respiratory Rate and weight assessed as not clinically significant (NCS) and afebrile as per PI/Sub-assessment. (Stable Vital signs will be re-assessed again prior to treatment with the SED on Day 2)
  • Able to perform and follow simple commands (ex: sit up in bed, lay down in bed)
  • Pre-Study CT/MRI Imaging stable per PI Sub-I Assessment post ventriculostomy.
  • Able to stand
  • Able to obtain consent

排除标准

  • Refractory ICP or needing active ICP management
  • Unable to tolerate brief clamping of EVD (<5min)
  • Unable to follow simple commands
  • Unconscious
  • Anticoagulant Therapy
  • Known bleeding diathesis
  • Scalp Infection
  • In the opinion of the Investigator the subject is not a good study candidate

研究组 & 干预措施

Single Arm study

Other

Single Arm study In this study, the subject will act as their own control. On Day 1 of the two day study, the subject will be observed while treated on their standard EVD. On Day 2, the subject will be treated with the Smart External Drain (SED).

干预措施: Smart External Drain - SED (Device)

结局指标

主要结局

Staff interactions

时间窗: Two Days

Average number of staff interactions per patient with standard EVD compared to intervention, the Smart External Drain (SED)

次要结局

  • Staff Time(Two Days)
  • Safety(Two Days)

研究者

发起方
Aqueduct Critical Care
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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