Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
NCT Number: NCT02422472
The purpose of this study is to compare ultrasound guided peripheral IV placement with and without the use of a guidewire. Patients in the Emergency Department with difficult peripheral IV access (as defined by 2 failed attempts by nursing staff) will be consented and randomized to standard ultrasound guided peripheral IV placement or ultrasound guided peripheral IV placement with modified seldinger technique using a guidewire.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Boston, Massachusetts, 02115, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Accucath™ 20 Gax 5.7cm catheter
Time frame: 60 minutes
First attempt success is defined as ability to place and use the catheter after only one attempt and will be reported by study staff.
Time frame: 60 minutes
Overall success is defined as ability to place and use the catheter (after 2 or fewer attempts) and will be reported by study staff.
Time frame: 60 minutes
Number of skin punctures will be recorded by study staff.
Time frame: 3 days
Patients will be monitored for complications of IV placement by study staff
Brigham and Women's Hospital
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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