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Clinical Trial Summary

The study will test a hypothesis that the AccuCathâ„¢ System will have a higher rate of successful first attempt peripheral IV placement and higher clinician and patient satisfaction compared to Conventional IV Catheters.


Clinical Trial Description

This study is designed to evaluate user/physician preference as it relates to use of a 510(k) cleared vascular access peripheral IV catheter device compared with peripheral IV conventional needle/catheter devices, in terms of first stick success rates, adverse events and overall user and patient satisfaction. As noted above, the study is designed to formally test the hypothesis that the AccuCathâ„¢ System will exhibit superiority in terms of the rate of successful first attempt peripheral IV placement and higher user and patient satisfaction compared to Conventional IV Catheters. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01940354
Study type Interventional
Source C. R. Bard
Contact
Status Completed
Phase N/A
Start date August 2013
Completion date March 2015

See also
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