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

Penn State Health logo

Penn State Health

Status

Completed

Conditions

Neuroscience ICU
PICC
Neuro ICU
CVC
Central Line
Central Venous Catheter

Treatments

Device: peripherally inserted central catheter
Device: centrally inserted central catheter

Study type

Interventional

Funder types

Other

Identifiers

NCT02314520
STUDY00000582

Details and patient eligibility

About

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.

Enrollment

152 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

152 participants in 2 patient groups

PICC
Active Comparator group
Description:
Patients randomly assigned to receive a peripherally inserted central catheter and they will be monitored for either having a complication or no complication.
Treatment:
Device: peripherally inserted central catheter
CVC
Active Comparator group
Description:
Patients randomly assigned to receive a centrally inserted central catheter and they will be monitored for either having a complication or no complication.
Treatment:
Device: centrally inserted central catheter

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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