Intravenous Access Clinical Trial
— AccuCathOfficial title:
Randomized, Controlled Study of Ultrasound-Guided Peripheral Venous Access Using AccuCath Versus Ultrasound-Guided Conventional Intravenous Catheter in the Emergency Department
NCT number | NCT02469038 |
Other study ID # | IRB15-0548 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2017 |
Est. completion date | June 2018 |
Verified date | December 2020 |
Source | University of Chicago |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
While peripheral venous cannulation is among the most common procedures performed in clinical settings, it is estimated that PIV insertion fails for 6 million patients annually. Failure to establish peripheral venous access in the emergency department is a costly problem, leading to delays in diagnostics and treatment and requiring alternative sites for vascular access. These alternative methods can lead to higher complications rates, decreased patient satisfaction, and increased utilization of nursing and physician time. Complications from PIV failure also pose a significant financial burden to the healthcare system. Ultrasound guidance has been shown to greatly improve the process of localizing vessels for cannulation. In a healthcare climate that is increasingly focused on outcomes and cost-effectiveness, ultrasound-guided peripheral venous cannulation has become not only a viable but often the preferred method in patients with difficult venous access. Nevertheless, studies to date on ultrasound-guided peripheral venous cannulation have revealed some shortcomings, such as premature failure and low first attempt success rates. The purpose of our study is to assess whether ultrasound-guided cannulation of a AccuCath catheter, which has a coiled tip guidewire, is superior to ultrasound-guided cannulation of a conventional peripheral IV catheter across clinical outcomes relevant to the emergency department setting.
Status | Completed |
Enrollment | 50 |
Est. completion date | June 2018 |
Est. primary completion date | June 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adult patients with IV access need Exclusion Criteria: - Lack of decisional capacity (e.g., intoxication, dementia, delirium, developmental delay), prior venous grafts or surgery at target IV site, not an acceptable candidate for ultrasound-guided PIV per Mitchell ED protocol (i.e. 3 failed attempts by nurses- 2 by primary nurse, 1 by senior nurse) |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Chicago |
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* Note: There are 21 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Total Number of Percutaneous Punctures | Total number of percutaneous punctures required for successful cannulation | During length of stay in emergency room up to 24 hours | |
Other | Total Number of IV Catheters | Total number of IV catheters required for successful cannulation | During length of stay in emergency room up to 24 hours | |
Other | Patient Satisfaction Data | Patient satisfaction data with each catheter system on a 5-point Likert scale minimum value=1, maximum value=5, higher scores are a better outcome | During length of stay in emergency room up to 24 hours | |
Other | Provider Satisfaction Data | Provider satisfaction data with each catheter system on a 5-point Likert scale minimum value=1, maximum value=5, higher scores are a better outcome | During length of stay in emergency room up to 24 hours | |
Other | Clinical and Demographic Information | medical history | During length of stay in emergency room up to 24 hours | |
Primary | First Attempt Success Rate | Rate of success of first attempt for IV access | During length of stay in emergency room up to 24 hours | |
Secondary | IV Procedure Time | Procedure time from the point of first percutaneous puncture to successful cannulation | During length of stay in emergency room up to 24 hours |
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