Nosocomial Infections Clinical Trial
Official title:
Impact of Daily Bathing With Chlorhexidine Impregnated Cloths on Nosocomial Infections in the Pediatric Intensive Care Unit
Verified date | September 2015 |
Source | Johns Hopkins University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
The investigators propose to conduct a large clinical study to determine if daily bathing with chlorhexidine impregnated cloths will reduce the incidence of healthcare-associated infections in the Pediatric Intensive Care Unit (PICU).
Status | Completed |
Enrollment | 5659 |
Est. completion date | June 2012 |
Est. primary completion date | December 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 2 Months to 25 Years |
Eligibility |
Inclusion Criteria: - Patients in pediatric intensive care unit Exclusion Criteria: - Patients with a history of an allergic reaction to chlorhexidine - Patients less than 2 months of age - Patients with severe skin disease or burn - Patients with an indwelling epidural catheter or lumbar drain |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Johns Hopkins Hospital | Baltimore | Maryland |
United States | Children's Hospital of Philadelphia | Philadelphia | Pennsylvania |
United States | Saint Louis Children's Hospital | Saint Louis | Missouri |
United States | Seattle Children's Hospital | Seattle | Washington |
United States | Children's National Medical Center | Washington | District of Columbia |
Lead Sponsor | Collaborator |
---|---|
Johns Hopkins University | Sage Products, Inc. |
United States,
Milstone AM, Elward A, Song X, Zerr DM, Orscheln R, Speck K, Obeng D, Reich NG, Coffin SE, Perl TM; Pediatric SCRUB Trial Study Group. Daily chlorhexidine bathing to reduce bacteraemia in critically ill children: a multicentre, cluster-randomised, crossov — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Bacteremia | per protocol analysis of incidence of bacteremia comparing those in treatment and control groups | duration of ICU stay, median 3 days | No |
Primary | Bacteremia | incidence of bacteremia comparing those in treatment and control groups | participants were followed for the duration of ICU stay, median stay 3 days | No |
Secondary | Central Line Associated-bloodstream Infection (CLABSI) | Comparing incidence of central line-associated bloodstream infections between treatment and control groups | participants were followed for the duration of ICU stay, median stay 3 days | No |
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