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Ultrasound IV Study

Christiana Care Health Services logo

Christiana Care Health Services

Status

Completed

Conditions

Ultrasound Use
IV Access

Treatments

Procedure: length of IV catheter

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to compare catheter length and extravasation rates for Ultrasound (US)-guided peripheral intravenous (IV) catheter insertion in a subset of emergency department patients with difficult IV access. Physicians, Emergency RNs, and Emergency Technicians can be taught to use US guidance to start peripheral IV in the ED. The optimal length of catheter to use for this procedure is unknown. This study will provide data on the length of catheter required to minimize extravasation. There is no guideline on catheter length selection for US-guided peripheral vascular access. This study may decrease extravasation rates for US-guided peripheral vascular access by providing guidance on catheter length selection.

Full description

The purpose of this study is to compare catheter length and extravasation rates for US guided peripheral IV insertion in a subset of emergency department patients with difficult IV access. Physicians, Emergency RNs, and Emergency Technicians can be taught to use US guidance to start peripheral IV in the ED. The optimal length of catheter to use for this procedure is unknown. This study will provide data on the length of catheter required to minimize extravasation. There is no guideline on catheter length selection for US-guided peripheral vascular access. This study may decrease extravasation rates for US-guided peripheral vascular access by providing guidance on catheter length selection.

The study design is a randomized non-blinded clinical trial of extravasation rates of US guided peripheral vascular access related to intravenous catheter length and venous depth in the ED. Primary endpoint is duration of usable vascular access. Secondary endpoints are catheter length, venous depth, time of procedure, successful cannulation, reasons for failure, number of skin punctures, site of cannulation, sonographic technique, type of provider obtaining access and complications.

Enrollment

22 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • two failed traditional IV attempts by a nurse
  • need for IV access as determined by the treating physician
  • age 18 and greater

Exclusion criteria

  • less than age 18
  • subjects needing a central venous catheter
  • patients unable to provide informed consent

Trial design

22 participants in 2 patient groups

1.75 inch catheter length
Active Comparator group
Description:
Length of catheter to be used
Treatment:
Procedure: length of IV catheter
2.5 inch catheter length
Active Comparator group
Description:
length of catheter to be used
Treatment:
Procedure: length of IV catheter

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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