Peripherally Inserted Central Catheter Placement by IV Team Nurses Using the Sonic Flashlight

Sponsor
University of Pittsburgh (Other)
Overall Status
Completed
CT.gov ID
NCT00226226
Collaborator
National Institutes of Health (NIH) (NIH)
230
1
12
19.2

Study Details

Study Description

Brief Summary

The purpose of this study is to test whether peripherally inserted central catheters can be safely placed on patients by intravenous team nurses at the bedside.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Peripherally Inserted Central Catheter Placement
Phase 1

Detailed Description

We have developed a new device for guiding invasive procedures with ultrasound (US), which we call the Sonic Flashlight (SF). We attach a half-silvered mirror and a small flat-panel monitor directly to an ultrasound transducer to project a virtual image of the US scan into its actual location within the patient. This permits the operator to guide a needle through the skin by aiming directly at the image, using natural hand-eye coordination rather than looking away from the patient at a conventional display. We believe the SF will increase accuracy, safety, and speed for a wide variety of invasive procedures and yield a faster learning of these procedures than conventional US displays.

The research proposed here would bring the application of guided needle insertion to its clinical implementation, specifically addressing the placement of the Peripherally Inserted Central Catheter (PICC) line. The PICC line is increasingly viewed as a safe alternative to direct central line placement in the jugular, subclavian, and femoral veins, while being easier to maintain than a peripheral intravenous line. This study will test the hypothesis that PICC lines can be placed by experienced intravenous (IV) team nurses using the SF for real-time US guidance.

Thirty nurse participants (ages 18-65) will be recruited from the IV team at UPMC Presbyterian Hospital to participate in the study. 200 patient subjects will be recruited from the adult (18 years and older) population of patients already scheduled to receive the PICC placement procedure; patients will have the lines placed by experienced IV team nurses using ultrasound guidance with either the SF or conventional ultrasound (CUS). Investigators will observe each procedure, using audio and video recording, ultrasound image data, and other characteristics of the procedure to monitor the success of each procedure. A set of feasibility trials will be conducted in the interventional radiology (IR) suite to assess the level of training the nurses have received prior to the start of the comparison trial.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
230 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Peripherally Inserted Central Catheter Placement by IV Team Nurses Using the Sonic Flashlight
Study Start Date :
Jun 1, 2006
Actual Study Completion Date :
Jun 1, 2007

Outcome Measures

Primary Outcome Measures

  1. PICC line successfully placed by intravenous team nurses using the Sonic Flashlight []

Secondary Outcome Measures

  1. PICC line successfully placed by intravenous team nurses using conventional ultrasound []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18 or older

  • Undergoing peripherally inserted central catheter placement as standard of care.

Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Pittsburgh Medical Center Pittsburgh Pennsylvania United States 15260

Sponsors and Collaborators

  • University of Pittsburgh
  • National Institutes of Health (NIH)

Investigators

  • Principal Investigator: George D Stetten, MD, PhD, University of Pittsburgh

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00226226
Other Study ID Numbers:
  • 0506042
First Posted:
Sep 26, 2005
Last Update Posted:
Feb 15, 2008
Last Verified:
Feb 1, 2008

Study Results

No Results Posted as of Feb 15, 2008