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

NCT ID: NCT02314520

Last Updated: 2017-07-19

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

152 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-07-13

Study Completion Date

2016-12-07

Brief Summary

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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.

Detailed Description

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Conditions

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PICC Central Venous Catheter Central Line Neuro ICU Neuroscience ICU CVC

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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PICC

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

Group Type ACTIVE_COMPARATOR

peripherally inserted central catheter

Intervention Type DEVICE

Any complication associated with central access

CVC

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

Group Type ACTIVE_COMPARATOR

centrally inserted central catheter

Intervention Type DEVICE

Central access not associated with any complication

Interventions

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peripherally inserted central catheter

Any complication associated with central access

Intervention Type DEVICE

centrally inserted central catheter

Central access not associated with any complication

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

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

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Milton S. Hershey Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Chris Zacko

Assistant Professor of Neurosurgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Penn State Hershey Medical Center

Hershey, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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STUDY00000582

Identifier Type: -

Identifier Source: org_study_id

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