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N/A N=35 Other

Ultrasound-guided Peripheral IJ Study

IV Access

Enrolled (actual)
35
Serious AEs
0.0%
Results posted
Jan 2019
Primary outcome: Primary: Number of Participants With Successful Cannulation of the Internal Jugular Vein — 34 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
US guided IJ (Procedure); Ultrasound (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University Medical Center of Southern Nevada
Primary completion
Sep 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Successful Cannulation of the Internal Jugular Vein
34
SECONDARY
Prevalence of Complications Related to Cannulation of the Internal Jugular Vein.
1
SECONDARY
The Median Time Required for Cannulation of the Internal Jugular Vein by an Emergency Physician.
3.1

Summary

Difficult venous access in some patients such as those with obesity, IV drug use, chronic illness, or vascular pathology often causes increased discomfort and delayed patient care due to multiple attempts to gain venous access. If access is achieved at all, it usually results in a much smaller catheter than needed to provide optimal care for the patient. Ultrasound-guided placement of a peripheral IV in the internal jugular vein is common in the investigators' emergency department and is gaining popularity across the US. This study investigates the utility and safety of placing an ultrasound-guided peripheral IV catheter in the internal jugular vein.

Eligibility Criteria

Inclusion Criteria

  • At least 2 unsuccessful attempts at peripheral IV access by ED nursing
  • Age 18 or older

Exclusion Criteria

  • Critically ill patients with clinical indications for emergent central venous access.
  • Overlying skin infection
  • External jugular vein easily visible for cannulation
  • Patient in law enforcement custody
  • Patient who is known to be pregnant or self identifies as pregnant
  • Patient lacking decision making capacity
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03231345). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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