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Topical Umbilical Cord Care for the Prevention of Colonization and Invasive Infections

Primary Purpose

Colonization

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Povidone-Iodine
Chlorhexidine
Pluronic
Control
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colonization focused on measuring Newborn Intensive Care Unit, Neonatal Intensive Care Unit, Colonization, Line Colonization, Umbilical line, Umbilical Cord Care

Eligibility Criteria

undefined - 7 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

*≤7 days of life

*Umbilical line(s) in place (UAC and/or UVC)

Exclusion Criteria:

*Not meeting inclusion criteria

Sites / Locations

  • Univeristy of Virginia Health System

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Sham Comparator

Arm Label

Povidone-Iodine (Betadine)

Chlorhexidine

Pluronic

Control (no application)

Arm Description

Umbilical stump care. Povidone-Iodine, USP, Swabstick Singles, applied once a day to cord stump while umbilical line(s) are in place

Umbilical stump care. ChloraPrep® Chlorhexidine Gluconate 2% w/v; 70% Isopropyl Alcohol v/v Swabstick Single, applied once a day to cord stump while umbilical line(s) are in place

Umbilical stump care. Pluronic gel - (F68, Polymyxin, Nystatin, Nitrofurantoin )applied once a day to cord stump while umbilical line(s) are in place

Control arm, no product is applied, which is standard of care.

Outcomes

Primary Outcome Measures

Colonization of umbilical stump

Secondary Outcome Measures

Late-onset infection
Late-onset infections include BSI, urinary tract infection (UTI), and meningitis. Catheter associated blood stream infections (CLABSI) for this study will be defined as growth in 1 or more blood cultures of any organism including CONS during or within 48-72 hours of having a central line in place, with signs and symptoms of sepsis, and treated for 7 days. Additionally we will compare the CDC definition of CLABSI between groups, and length of stay (LOS).
contact dermatitis
Skin irritation around the umbilical stump

Full Information

First Posted
June 17, 2013
Last Updated
April 30, 2018
Sponsor
University of Virginia
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1. Study Identification

Unique Protocol Identification Number
NCT01886001
Brief Title
Topical Umbilical Cord Care for the Prevention of Colonization and Invasive Infections
Official Title
Topical Umbilical Cord Care for the Prevention of Colonization and Invasive Infections
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Umbilical catheters are necessary for many infants admitted to the Newborn Intensive Care Unit (NICU)and utilized when indicated for up to 7 to 14 days. Bacterial colonization can occur at the umbilical stump and potentially lead to serious bloodstream infections (BSIs). This study is a prospective, randomized controlled feasibility trial to evaluate three types of hygiene products on umbilical line stumps, on the effect of line colonization and subsequent infections. Infants admitted to the NICU with an umbilical line(s) will be randomized into one of four study groups, three products against standard of care (no product). The three products that will be evaluated are currently being used in different capacities for skin care in the UVA NICU. The study hypothesizes that daily topical application of 1 or more antiseptic to the top of the umbilical stump will decrease colonization of the umbilical stump while umbilical lines are in place.
Detailed Description
Umbilical catheter associated infections are higher (4.4 vs. 3.4 CLABSIs per 1000 line days) than other central lines such as PICCs and surgically placed CVLin the NICU. (www.CDC.gov - NSHN 2010 Report). Routine care of the skin entry site (e.g. central line dressing care) is standard for other central lines, but there is no standard for care of the umbilical stump while umbilical lines are in place. In a pilot study to evaluate the relationship of umbilical stump colonization with gestational age, the number of days the catheter was in place, and the type of organisms, colonization was detected in 78% of patients. There was a direct correlation with colonization and line days as well as an inverse relationship with lower gestational age. This pilot data supported the need for the study of interventions to reduce umbilical stump colonization, which may help decrease blood stream infections (BSIs) associated with umbilical lines in the NICU. The proposed study will evaluate feasibility of once daily product application.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colonization
Keywords
Newborn Intensive Care Unit, Neonatal Intensive Care Unit, Colonization, Line Colonization, Umbilical line, Umbilical Cord Care

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Povidone-Iodine (Betadine)
Arm Type
Experimental
Arm Description
Umbilical stump care. Povidone-Iodine, USP, Swabstick Singles, applied once a day to cord stump while umbilical line(s) are in place
Arm Title
Chlorhexidine
Arm Type
Experimental
Arm Description
Umbilical stump care. ChloraPrep® Chlorhexidine Gluconate 2% w/v; 70% Isopropyl Alcohol v/v Swabstick Single, applied once a day to cord stump while umbilical line(s) are in place
Arm Title
Pluronic
Arm Type
Experimental
Arm Description
Umbilical stump care. Pluronic gel - (F68, Polymyxin, Nystatin, Nitrofurantoin )applied once a day to cord stump while umbilical line(s) are in place
Arm Title
Control (no application)
Arm Type
Sham Comparator
Arm Description
Control arm, no product is applied, which is standard of care.
Intervention Type
Drug
Intervention Name(s)
Povidone-Iodine
Other Intervention Name(s)
Betadine
Intervention Description
Umbilical stump care. Povidone-Iodine, USP, Swabstick Singles, applied once a day to cord stump while umbilical line(s) are in place
Intervention Type
Drug
Intervention Name(s)
Chlorhexidine
Other Intervention Name(s)
ChloraPrep®, Chlorhexidine Gluconate 2% w/v;70% Isopropyl Alcohol
Intervention Description
Umbilical stump care. Chlorhexidine Gluconate 2% w/v; 70% Isopropyl Alcohol v/v Swabstick Single, applied once a day to cord stump while umbilical line(s) are in place
Intervention Type
Drug
Intervention Name(s)
Pluronic
Other Intervention Name(s)
Pluronic Gel
Intervention Description
Umbilical stump care. Pluronic gel - (F68, Polymyxin, Nystatin, Nitrofurantoin)applied once a day to cord stump while umbilical line(s) are in place
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
No product is applied to cord stump while umbilical line(s) are in place. This is the current standard of care at UVA.
Primary Outcome Measure Information:
Title
Colonization of umbilical stump
Time Frame
while umbilical lines are in place which is an average of 7 days
Secondary Outcome Measure Information:
Title
Late-onset infection
Description
Late-onset infections include BSI, urinary tract infection (UTI), and meningitis. Catheter associated blood stream infections (CLABSI) for this study will be defined as growth in 1 or more blood cultures of any organism including CONS during or within 48-72 hours of having a central line in place, with signs and symptoms of sepsis, and treated for 7 days. Additionally we will compare the CDC definition of CLABSI between groups, and length of stay (LOS).
Time Frame
up to 120 days of life, transfer, death or discharge from NICU
Title
contact dermatitis
Description
Skin irritation around the umbilical stump
Time Frame
during intervention which is an average of 7 days

10. Eligibility

Sex
All
Maximum Age & Unit of Time
7 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: *≤7 days of life *Umbilical line(s) in place (UAC and/or UVC) Exclusion Criteria: *Not meeting inclusion criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David A Kaufman, MD
Organizational Affiliation
UVA School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Univeristy of Virginia Health System
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
plan to analyze data and publish

Learn more about this trial

Topical Umbilical Cord Care for the Prevention of Colonization and Invasive Infections

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