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Umbilical Cord Care for the Prevention of Colonization

Primary Purpose

Line Insertion Site, Central Line-associated Bloodstream Infection (CLABSI)

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Povidone-Iodine
Chlorhexidine gluconate
Pluronic Cream
control
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Line Insertion Site focused on measuring Prematurity, Central line care, Umbilical line colonization, Colonization, Newborn Intensive Care Unit, Neonatal Intensive Care Unit

Eligibility Criteria

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

Inclusion Criteria:

*≤7 days of life

*Umbilical line(s) in place (Umbilical arterial catheter=UAC and/or Umbilical venous catheter=UVC)

Exclusion Criteria:

*Not meeting inclusion criteria

Sites / Locations

  • University of Virginia HealthSystemRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Sham Comparator

Arm Label

Povidone-Iodine

Chlorhexidine

Pluronic Cream

Control

Arm Description

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

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

No product is applied to cord stump while umbilical line(s) are in place. This is the current standard of care at UVA.

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 of cord or skin base

Full Information

First Posted
June 20, 2013
Last Updated
August 1, 2013
Sponsor
University of Virginia
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1. Study Identification

Unique Protocol Identification Number
NCT01893060
Brief Title
Umbilical Cord Care for the Prevention of Colonization
Official Title
Umbilical Cord Care for the Prevention of Colonization
Study Type
Interventional

2. Study Status

Record Verification Date
August 2013
Overall Recruitment Status
Unknown status
Study Start Date
July 2013 (undefined)
Primary Completion Date
May 2014 (Anticipated)
Study Completion Date
July 2014 (Anticipated)

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 University of Virginia (UVA) NICU. The study hypothesizes that twice 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 peripherally inserted central catheters (PICCs) and surgically placed central venous lines (CVL) in 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 twice daily product application.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Line Insertion Site, Central Line-associated Bloodstream Infection (CLABSI)
Keywords
Prematurity, Central line care, Umbilical line colonization, Colonization, Newborn Intensive Care Unit, Neonatal Intensive Care Unit

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Povidone-Iodine
Arm Type
Experimental
Arm Description
Umbilical stump care. Povidone-Iodine, USP, Swabstick Singles, applied twice 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 twice a day to cord stump while umbilical line(s) are in place
Arm Title
Pluronic Cream
Arm Type
Experimental
Arm Description
Umbilical stump care. Pluronic gel - (F68, Polymyxin, Nystatin, Nitrofurantoin), applied twice a day to cord stump while umbilical line(s) are in place
Arm Title
Control
Arm Type
Sham Comparator
Arm Description
No product is applied to cord stump while umbilical line(s) are in place. This is the current standard of care at UVA.
Intervention Type
Drug
Intervention Name(s)
Povidone-Iodine
Other Intervention Name(s)
Betadine
Intervention Description
Povidone-Iodine, USP, Swabstick Singles, applied twice a day to cord stump while umbilical line(s) are in place
Intervention Type
Drug
Intervention Name(s)
Chlorhexidine gluconate
Other Intervention Name(s)
ChloraPrep®
Intervention Description
Chlorhexidine Gluconate 2% w/v; 70% Isopropyl Alcohol v/v Swabstick Single, applied twice a day to cord stump while umbilical line(s) are in place
Intervention Type
Drug
Intervention Name(s)
Pluronic Cream
Other Intervention Name(s)
Pluronic Gel, Pluronic
Intervention Description
Pluronic cream - (F68, Polymyxin, Nystatin, Nitrofurantoin )applied twice a day to cord stump while umbilical line(s) are in place
Intervention Type
Other
Intervention Name(s)
control
Other Intervention Name(s)
Sham 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, 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 of cord or skin base
Time Frame
while lines are in place, 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 (Umbilical arterial catheter=UAC and/or Umbilical venous catheter=UVC) Exclusion Criteria: *Not meeting inclusion criteria
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David A Kaufman, MD
Phone
434-924-9114
Email
dak4r@virginia.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Amy E Blackman, BSN
Phone
434-982-0263
Email
as5v@virginia.edu
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
University of Virginia HealthSystem
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22932
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David A Kaufman, MD
Phone
434-924-5428
Email
dak4r@virginia.edu
First Name & Middle Initial & Last Name & Degree
Amy E. Blackman, MD
Phone
434-982-0263
Email
as5v@virginia.edu

12. IPD Sharing Statement

Learn more about this trial

Umbilical Cord Care for the Prevention of Colonization

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