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

Sponsor
University of Virginia (Other)
Overall Status
Completed
CT.gov ID
NCT01886001
Collaborator
(none)
53
1
4
8
6.7

Study Details

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.

Condition or Disease Intervention/Treatment Phase
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
53 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Topical Umbilical Cord Care for the Prevention of Colonization and Invasive Infections
Study Start Date :
Nov 1, 2012
Actual Primary Completion Date :
May 1, 2013
Actual Study Completion Date :
Jul 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Povidone-Iodine (Betadine)

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

Drug: Povidone-Iodine
Umbilical stump care. Povidone-Iodine, USP, Swabstick Singles, applied once a day to cord stump while umbilical line(s) are in place
Other Names:
  • Betadine
  • Experimental: Chlorhexidine

    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

    Drug: Chlorhexidine
    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
    Other Names:
  • ChloraPrep®
  • Chlorhexidine Gluconate 2% w/v;70% Isopropyl Alcohol
  • Experimental: Pluronic

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

    Drug: Pluronic
    Umbilical stump care. Pluronic gel - (F68, Polymyxin, Nystatin, Nitrofurantoin)applied once a day to cord stump while umbilical line(s) are in place
    Other Names:
  • Pluronic Gel
  • Sham Comparator: Control (no application)

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

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

    Outcome Measures

    Primary Outcome Measures

    1. Colonization of umbilical stump [while umbilical lines are in place which is an average of 7 days]

    Secondary Outcome Measures

    1. Late-onset infection [up to 120 days of life, transfer, death or discharge from NICU]

      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).

    2. contact dermatitis [during intervention which is an average of 7 days]

      Skin irritation around the umbilical stump

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 7 Days
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    *≤7 days of life

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

    Exclusion Criteria:

    *Not meeting inclusion criteria

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Univeristy of Virginia Health System Charlottesville Virginia United States 22908

    Sponsors and Collaborators

    • University of Virginia

    Investigators

    • Principal Investigator: David A Kaufman, MD, UVA School of Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    David A Kaufman, Medical Doctor, University of Virginia
    ClinicalTrials.gov Identifier:
    NCT01886001
    Other Study ID Numbers:
    • 16396
    First Posted:
    Jun 25, 2013
    Last Update Posted:
    May 3, 2018
    Last Verified:
    Apr 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by David A Kaufman, Medical Doctor, University of Virginia
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 3, 2018