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CompletedNCT02584530Updated Jul 30, 2020

Comparing Ultrasound Guided PICC Line Insertion in Neonates With Standard Procedure

An interventional study of Ultrasound guidance for PICC line placement in Ultrasonography, Interventional and Peripheral Venous Catheterization, sponsored by Children's Hospital of Eastern Ontario. Completed at 1 site in Canada. Open to participants aged 1 Day to 28 Days. Per ClinicalTrials.gov, last updated 2020-07-30.

Sponsored by Children's Hospital of Eastern Ontario · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
1 Day to 28 Days
Sex
All
01

Study summary

This is a randomized controlled study comparing US guided vs standard procedure for PICC line placement in newborns admitted to Children's Hospital of Eastern Ontario Neonatal Intensive Care Unit who require a PICC line. Patients will be randomized using REDCap randomization module (stratified by gestational age \< 28 weeks and >= 28 weeks and blocked to ensure approximate balance with each stratum) into two arms. - Arm 1: PICC line insertion procedure using anatomical landmarks and tip placement will be confirmed by X-ray (current standard); Arm 2: US guided PICC line insertion procedure and tip placement confirmation by both US and X-ray. Sample size of 33 infants per group would achieve greater than 80% power to detect a difference between groups.

Primary outcome: Time to complete the standard versus the US-guided procedure.

Secondary outcomes (comparison between two arms):

The number of total "venipuncture" attempts needed to place a PICC line Number of tip manipulations after complete insertion Proportion of successful tip placement

Read the detailed description

Background Peripherally Inserted Central Catheter (PICC) line placement is one of the most commonly performed procedures in Neonatology. Due to prematurity and small vein size, the procedure often requires multiple attempts over an increased timeframe. As a standard of care, the position is confirmed by X-ray. Frequently, catheters are not optimally positioned, necessitating repositioning and further radiographs.

The use of ultrasound (US) guidance for PICC line placement enhances the visualization of the veins and provides a better selection for optimal access. It could decrease or even eliminate the need for X-rays when used to confirm the tip position.

Objectives To demonstrate that using US-guidance to place and confirm tip positioning for PICC line insertion in neonates will decrease the number of cannulation attempts, will shorten the time needed to complete the procedure, and will decrease infants' exposure to radiation.

Methods This is a randomized controlled study comparing US guided vs standard procedure for PICC line placement in newborns admitted to CHEO NICU who require a PICC line (approximately 130-150 infants per year). Patients will be randomized using REDCap randomization module (stratified by gestational age \< 28 weeks and >= 28 weeks and blocked to ensure approximate balance with each stratum) into two arms - Arm 1: PICC line insertion procedure using anatomical landmarks and tip placement will be confirmed by X-ray (current standard); Arm 2: US guided PICC line insertion procedure and tip placement confirmation by both US and X-ray. A sample size of 33 infants per group would be sufficient to achieve greater than 80% power to detect a difference between groups.

Results of this study may demonstrate that US guided PICC line placement is superior (shorter and safer procedure, reduced radiation and pain) to currently used procedure and could lead to practice change.

02

Conditions studied

  • Ultrasonography, Interventional
  • Peripheral Venous Catheterization

Keywords

  • ultrasound
  • PICC line
  • neonate
03

In context

Lead sponsor

Children's Hospital of Eastern Ontario is the lead sponsor of 83 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Day to 28 Days
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

All newborns (0-28 days) admitted to Neonatal Intensive Care Unit who require PICC line insertion after consent has been obtained to include in this study. Including:

  • Infants who need prolonged Total Parenteral Nutrition requirement of > 7 days.
  • Infants with difficult peripheral venous access who requires a central line
  • Infants who require IV medications for > 7 days.
  • Infants who require medications given by central IV access
  • Infants who will undergo complex surgical procedures and will require central IV access before procedure.

Exclusion criteria

Exclusion Criteria:

  • Infants requiring isolation according to infection control protocols
  • Unable to obtain or refused consent for PICC line and/or study enrolment
  • Infants with any clinical contraindication for PICC line insertion as per unit policy
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • No intervention
    Standard procedure group

    PICC line insertion using anatomical landmarks guidance and tip placement confirmation by X-ray

  • Experimental
    Interventional group

    Ultrasound guidance for PICC line placement and X-ray

    Procedure: Ultrasound guidance for PICC line placement

Interventions

  • ProcedureUltrasound guidance for PICC line placement

    Apply ultrasound guidance for PICC line placement and positioning in newborns

06

What researchers measure

Primary outcomes

  1. Time to complete the standard versus the US-guided procedure

    Comparison between total time of procedure with standard approach vs US guidance measured in minutes.

    Time frame: one year

Secondary outcomes

  1. Number of total venipuncture attempts needed to place a PICC line

    Number of venipuncture attempts will be documented per patient through the whole duration of study and then both groups will be compared differences in number

    Time frame: One year

  2. Number of tip manipulations after complete insertion

    Number of manipulations of tip line for adequate placement will be documented on each patient and then compared against control group to assess for differences in number.

    Time frame: One year

  3. Proportion of successful tip placement

    Total number of correct position of PICC line tip will be documented in both groups and then compared to control.

    Time frame: One year

07

Study locations

1 site
  • Children's Hospital of Eastern Ontario
    Ottawa, Ontario K1H8L1, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02584530
Lead sponsor
Children's Hospital of Eastern Ontario
Responsible party
Nadya Ben Fadel (Neonatologist, Children's Hospital of Eastern Ontario) — Principal investigator
First posted
Oct 22, 2015
Start date
Jul 2016
Primary completion
Mar 30, 2020
Completion
Mar 30, 2020
Last update
Jul 30, 2020

Study contacts

Nadya Ben Fadel, MD
principal investigator · Children's Hospital of Eastern Ontario

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2020. You cannot join it, but the record below documents what was studied.

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