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Use of Vein Viewer for Insertion of Peripheral Venous Cannula in Pediatric Patients With Difficult Intravenous Access

NCT00935909 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 603

Last updated 2013-06-21

No results posted yet for this study

Summary

The primary purpose of this prospective, randomized trial is successful intravenous (IV) cannulation on first attempt with the use of either the Vein Viewer (VV) or standard cannulation method. The secondary purpose is to find out if there is a difference in the total time to successful cannulation.

Conditions

  • IV Cannulation

Sponsors & Collaborators

  • Luminex Corporation

    collaborator INDUSTRY

  • Outcomes Research Consortium

    collaborator OTHER

  • Peter Szmuk

    lead OTHER

Principal Investigators

  • Peter Szmuk, MD · UT Southwestern

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2010-07-31
Completion
2010-07-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00935909 on ClinicalTrials.gov