跳至主要内容
临床试验/NCT02314520
NCT02314520已完成不适用

Complications Associated With Central Venous Access in the NSICU: PICC vs CVC

Milton S. Hershey Medical Center2 个研究点 分布在 1 个国家目标入组 152 人开始时间: 2015年7月13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
入组人数
152
试验地点
2
主要终点
Participants With Complications With Central Access Including Insertion

研究概览

简要总结

The goal of this study is to determine whether Peripherally Inserted Central Catheter or Centrally Inserted Venous Catheters have lower complication rates in the Neuroscience Intensive Care Unit. After admission to the Neuroscience ICU and if they require central access, patients will be randomized to receive a PICC or CVC and complications (such as pneumothorax, deep venous thrombosis, infection, etc.) will be tracked and compared between the two interventions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

  • Adult patients admitted to the NSICU, who require central access for the treatment of their illness.

排除标准

  • Current or recent (within 1 month) diagnosis of bacteremia
  • Current or recent (within 1 year with confirmed resolution by imaging) deep venous thrombosis
  • Existing central access
  • Non-English speaking
  • Requirement for emergent central access and unable to obtain consent in an emergency setting

研究组 & 干预措施

PICC

Active Comparator

Patients randomly assigned to receive a peripherally inserted central catheter and they will be monitored for either having a complication or no complication.

干预措施: peripherally inserted central catheter (Device)

CVC

Active Comparator

Patients randomly assigned to receive a centrally inserted central catheter and they will be monitored for either having a complication or no complication.

干预措施: centrally inserted central catheter (Device)

结局指标

主要结局

Participants With Complications With Central Access Including Insertion

时间窗: up to 10 weeks

Aggregation of all complications associated with central access including insertion

次要结局

  • Number of Participants With Deep Venous Thrombosis(up to 10 weeks)
  • Number of Patients With Complications Related to Insertion(From the time of insertion until first confirmatory chest X-ray)
  • Number of Participants With a Central Line Associated Blood Stream Infection(up to 10 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chris Zacko

Assistant Professor of Neurosurgery

Milton S. Hershey Medical Center

研究点 (2)

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