Colonization Clinical Trial
Official title:
Topical Umbilical Cord Care for the Prevention of Colonization and Invasive Infections
NCT number | NCT01886001 |
Other study ID # | 16396 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2012 |
Est. completion date | July 2013 |
Verified date | April 2018 |
Source | University of Virginia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 53 |
Est. completion date | July 2013 |
Est. primary completion date | May 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A to 7 Days |
Eligibility |
Inclusion Criteria: *=7 days of life *Umbilical line(s) in place (UAC and/or UVC) Exclusion Criteria: *Not meeting inclusion criteria |
Country | Name | City | State |
---|---|---|---|
United States | Univeristy of Virginia Health System | Charlottesville | Virginia |
Lead Sponsor | Collaborator |
---|---|
University of Virginia |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Colonization of umbilical stump | while umbilical lines are in place which is an average of 7 days | ||
Secondary | 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). | up to 120 days of life, transfer, death or discharge from NICU | |
Secondary | contact dermatitis | Skin irritation around the umbilical stump | during intervention which is an average of 7 days |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00520715 -
Epidemiology of Fluoroquinolone Resistance in Human Commensal Flora in Patients Hospitalised in Medical Wards
|
N/A | |
Completed |
NCT02260479 -
Preheated Skin Disinfection vs Room-temperature on Bacterial Colonization During Pace Device Implantation
|
Phase 2/Phase 3 | |
Completed |
NCT03479710 -
Fecal Microbiota Transplantation for CRE/VRE
|
Phase 2 |