Clinical Trials Logo

Clinical Trial 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.


Clinical Trial 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. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01893060
Study type Interventional
Source University of Virginia
Contact David A Kaufman, MD
Phone 434-924-9114
Email dak4r@virginia.edu
Status Recruiting
Phase N/A
Start date July 2013
Completion date July 2014

See also
  Status Clinical Trial Phase
Withdrawn NCT03282292 - Central Venous Catheter Insertion Site and Colonization in Pediatric Cardiac Surgery N/A
Recruiting NCT05740150 - Central Line-associated Bloodstream Infection Prevention Using TauroLock-Hep100 in Pediatric Oncology Patients. N/A
Completed NCT03898115 - Implementation Program to Improve CHG Bathing Compliance N/A
Recruiting NCT04548713 - CLiCK in the Critical Care Unit N/A
Completed NCT03253887 - Ethanol-lock Therapy for the Prevention of Non-tunneled Catheter-related Infection in Pediatric Patients Phase 3
Recruiting NCT05376566 - Hydrochloric Acid Lock Therapy for Central Line-associated Bloodstream Infections N/A
Not yet recruiting NCT04856878 - Effect of Vancomycin After Catheter Replacement Phase 4
Completed NCT00975923 - Safe Critical Care: Testing Improvement Strategies N/A
Enrolling by invitation NCT04559334 - Compassionate-Use of 4% T-EDTA Lock Solution for Central Venous Lines of Pediatric PN Patients N/A
Active, not recruiting NCT05485051 - Daily Chlorexidine Bath for Health Care Associated Infection Prevention Phase 3
Completed NCT03692559 - The Effects of Different Ways of Dressing Central Line Associated Bloodstream Infections N/A
Completed NCT02969343 - Patient Safety Learning Laboratory: Making Acute Care More Patient-Centered N/A
Completed NCT03486093 - Port Protectors for Prevention of CLABSIs in Respiratory Semi-intensive Care Unit N/A
Completed NCT05919966 - The Association Between Chlorhexidine Bathing and Central Line-Associated Infections in Medical Intensive Care Units