Comparing Ultrasound Guided PICC Line Insertion in Neonates With Standard Procedure

Sponsor
Children's Hospital of Eastern Ontario (Other)
Overall Status
Completed
CT.gov ID
NCT02584530
Collaborator
(none)
60
1
2
44.9
1.3

Study Details

Study Description

Brief 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

Condition or Disease Intervention/Treatment Phase
  • Procedure: Ultrasound guidance for PICC line placement
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
A Randomized Controlled Trial Comparing Ultrasound Guided PICC Line Insertion in Neonates With Standard Procedure
Actual Study Start Date :
Jul 1, 2016
Actual Primary Completion Date :
Mar 30, 2020
Actual Study Completion Date :
Mar 30, 2020

Arms and Interventions

Arm Intervention/Treatment
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
Apply ultrasound guidance for PICC line placement and positioning in newborns

Outcome Measures

Primary Outcome Measures

  1. Time to complete the standard versus the US-guided procedure [one year]

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

Secondary Outcome Measures

  1. Number of total venipuncture attempts needed to place a PICC line [One year]

    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

  2. Number of tip manipulations after complete insertion [One year]

    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.

  3. Proportion of successful tip placement [One year]

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

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Day to 28 Days
Sexes Eligible for Study:
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:
  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Children's Hospital of Eastern Ontario Ottawa Ontario Canada K1H8L1

Sponsors and Collaborators

  • Children's Hospital of Eastern Ontario

Investigators

  • Principal Investigator: Nadya Ben Fadel, MD, Children's Hospital of Eastern Ontario

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nadya Ben Fadel, Neonatologist, Children's Hospital of Eastern Ontario
ClinicalTrials.gov Identifier:
NCT02584530
Other Study ID Numbers:
  • 20150456
First Posted:
Oct 22, 2015
Last Update Posted:
Jul 30, 2020
Last Verified:
Jul 1, 2020
Keywords provided by Nadya Ben Fadel, Neonatologist, Children's Hospital of Eastern Ontario

Study Results

No Results Posted as of Jul 30, 2020