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Completed

NCT Number: NCT04412967

Nurse-led Placement of Peripheral Venous Catheters in Overweight Patients Using Standard or Dynamic Ultrasound-guided Technique

Overweight and obesity may be associated with difficult intravenous access leading to longer procedure time and more placement attempts of peripheral venous catheters (PVC). Dynamic ultrasound-guided short-axis needle tip navigation (DUST) may facilitate the procedure.

This was a prospective, randomized, non-blinded study to compare time and placement attempts for nurse-led standard (ST) and ultrasound guided PVC placement in 90 emergency patients with a BMI ≥25kg/m2.

Consenting patients were randomized at a 1:1 ratio to receive PVC by either ST or DUST.

Application time was defined as the time from applying stasis to visible blood in the PVC flash-chamber.

No difference in time was found (medians: ST 42 s; DUST 53.5 s, P = 0.535). There were on average 17 % less placement attempts in the DUST-group (median 1 attempt; Q1 = 1 Q3 = 1) compared to the ST-group (median 1 attempt; Q1 = 1 Q3 = 1.5), (p = 0.031). Patients reported no differences in perceived pain (p = 0.955) or perceived satisfaction (p = 0.342). Pain and subcutaneous infiltrations were the only side-effects reported (ST-group 6, DUST-group 5).

DUST does not decrease time to functional PVC but reduces the number of PVC placement attempts in patients with BMI ≥25 kg/m2.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Linköping

Linköping, Östergötland County, 58185, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • REETS prioritization level of "Orange", "Yellow", "Green" or "Blue"
  • 18 years old
  • BMI ≥25 Kg/m2
  • Need of PVC according to Emergency department guidelines
  • Able to give written informed consent

Exclusion criteria

  • Unable or unwilling to provide informed consent
  • Life threatening patient status (REETS prioritization level of "Red")
  • Immunosuppression
  • Pregnant or lactating women
  • Blood infections
  • Puncture zone skin damaged (burns, eczema, infection)

Treatment and study plan

Dynamic ultrasound-guided short-axis needle tip navigation

Device

placement of peripheral venous catheters using ultrasound guided technique

Standard technique of placing a PVC

Other

Standard technique with palpation or Visual inspection of the pvc placement site

Primary outcomes

  1. Time to application

    Time frame: 1 hour

    Application time was defined as the time from applying stasis to visible blood in the PVC flash-chamber.

  2. Number of cannulation attempts

    Time frame: 1 hour

    The total number of cannulation attempts performed per patient

Secondary outcomes

  1. Patient satisfaction

    Time frame: 1 hour

    The perceived satisfaction of the patient as indicated by Numeric Rating scale (NRS, 0 = not satisfied, 10 = maximum satisfaction)

  2. Perceived Pain

    Time frame: 1 hour

    The perceived pain of the patient as indicated by Numeric Rating scale (NRS, 0 = no pain, 10 = the worst pain possible)

Sponsors and collaborators

Lead sponsor

University Hospital, Linkoeping

Other

Registry information

Official study title

A Randomized, Controlled Comparison of Nurse-led Placement of Peripheral Venous Catheters in Overweight Patients Using Standard or Dynamic Ultrasound-guided Technique

Acronym: DUST

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Jun 2, 2020
Registry last updated
Jun 30, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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