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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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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Standard | No Intervention | Standard of care ultrasound guided peripheral IV placement | |
| Experimental | Experimental | Ultrasound guided peripheral IV placement with the use of a guidewire |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ultrasound guided peripheral IV placement | Device | Accucathâ„¢ 20 Gax 5.7cm catheter |
|
| Measure | Description | Time Frame |
|---|---|---|
| First attempt success rate | First attempt success is defined as ability to place and use the catheter after only one attempt and will be reported by study staff. | 60 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| Overall success rate | Overall success is defined as ability to place and use the catheter (after 2 or fewer attempts) and will be reported by study staff. | 60 minutes |
| Number of skin punctures |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Heidi Kimberly, MD | Brigham and Women's Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Brigham and Women's Hospital | Boston | Massachusetts | 02115 | United States |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Feb 10, 2020 | |
| Reset | Feb 21, 2020 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Feb 10, 2020 | Feb 21, 2020 |
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Number of skin punctures will be recorded by study staff.
| 60 minutes |
| Complications including hematoma, IV infiltration, catheter dislodge | Patients will be monitored for complications of IV placement by study staff | 3 days |