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Peripheral Internal Jugular Vein ('Peripheral IJ') Access in Patients Identified as Difficult Intravenous Access

Peripheral Internal Jugular Vein ('Peripheral IJ') Access in Patients Identified as Difficult Intravenous Access Research Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03063996
Enrollment
29
Registered
2017-02-24
Start date
2017-02-07
Completion date
2018-06-12
Last updated
2018-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Difficult IV Access

Brief summary

The primary aim of this study is to determine if the insertion of a peripheral Internal Jugular (IJ) catheter is faster than a standard of care intravenous (IV)access in patients with difficult access. The secondary aims of this study examine patient discomfort between standard IV insertion vs. peripheral IV insertion as well as a comparison of complication rates between the two methods of insertion. Support for the peripheral IV procedure could provide an option for the thousands of Emergency Department (ED) patients who daily encounter the situation of difficult IV access and the numerous needle pokes that accompany it. Using this procedure may result in greater patient satisfaction and reduced complication rates.

Detailed description

This will be a randomized control trial comparing peripheral IJ to standard care of difficult access patients. 1. Patients will be identified by nurses as having difficult IV access. This can be determined based on past history or immediate experience. In other words, while a nurse is caring for a patient, s/he might notice that the patient looks to have difficult veins for an IV and may ask the patient 'Are you a hard stick?'. On the other hand, the nurse may fail at a number of attempts at placing an IV. In both of the cases, the patients can be determined to have difficult access and the nurse will have the option to contact the research assistant or continue with current attempts. 2. Nurse will contact research assistant. 3. Research assistant (RA) will determine if the patient is being cared for by an MD with appropriate experience for placing the peripheral IJ (attending, second or third year ED resident). 4. RA will consent patient, discussing possible continuation of IV or IJ catheter insertion. If patient agrees, he/she will be enrolled in the study. 5. Patient will be randomized. 6. Time clock will be started by RA when nurse or study member (attending physician, second or third year resident) start the procedure (IV or IJ). 7. RA will monitor procedure progress and stop time clock when access has been confirmed by study member or by nurse. 8. RA will survey patient regarding pain during procedure and satisfaction. 9. Patient chart will be queried at the completion of ED visit or hospitalization for complications. Chart will be queried again at two weeks to evaluate for any return visit complication. Catheters will be placed by attending physicians and residents (2nd and 3rd years) with experience placing ultrasound guided internal jugular central venous catheters. Because the procedure is identical to the first step of placing an IJ Central Venous Catheter, there is no special training needed for the procedure itself. A video will be created and viewed by all placing the catheters to show the specifics so that there is standardization between individuals. Attempts to place the peripheral IJ will be limited to two. If not successful after two attempts, the patient will return to 'standard care' and the treatment team will decide on further directions such as ultrasound guided peripheral IV or central venous line.

Interventions

PROCEDUREperipheral IV access procedure

standard of care guided IV access into peripheral vein excluding IJ

PROCEDUREPeripheral IJ access procedure

standard of care guided IV access into IJ

Sponsors

HealthPartners Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This will be a randomized control trial comparing peripheral IJ to standard care of difficult access patients.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Emergency Department patient 2. Need for IV access 3. Difficult access as determined by nurse based on current challenges with IV access or in discussion with patient regarding past experience 4. Patient in stable condition as determined by treating team 5. English speaking 6. Ability to consent 7. Age ≥ 18 years

Exclusion criteria

1. Prior neck surgery 2. Known blood clot in IJ vein 3. Overlying infection 4. Need for immediate IV access 5. Provider not available for procedure

Design outcomes

Primary

MeasureTime frameDescription
Total time to gain successful IV accessED arrival to successful venous access, up to 300 minutesTime to successful IV (or IJ) access in minutes from ED arrival

Secondary

MeasureTime frameDescription
Venous access complicationUp to 2 weeks after IV placement and/or removalVariables: Immediate Complications -noted at time of procedure (hematoma, arterial puncture, pneumothorax, infection, line failure) Delayed complications - noted at time of discharge OR at 2 week chart follow-up (hematoma, pneumothorax, infection, line failure)
Procedural patient comfortAverage 5 minutes to 1 hour post procedurePain-score assessment (10-point Likert scale)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026