Congenital Disorders Clinical Trial
Official title:
Frequency of Accessing Central Lines for Blood Samples and Medication Administration: A Comparison Between CICU, PICU and NICU
NCT number | NCT00366314 |
Other study ID # | 06-142 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | August 17, 2006 |
Last updated | June 12, 2007 |
Start date | June 2003 |
Verified date | June 2007 |
Source | Children's Healthcare of Atlanta |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Observational |
The purpose of this study is to quantify and analyze the line accesses for each of the 3
participating ICUs.
The hypothesis is that the CICU will have a significantly higher number of line accesses
than the other units. Analyzing the data will assist the researchers in identifying best
practices and ultimately, reduce the BSI rate in the CICU.
Status | Terminated |
Enrollment | 320 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A to 18 Years |
Eligibility |
Inclusion Criteria: - ICUs at Egleston Hospital, Children's Healthcare of Atlanta - June 1, 2003 - June 30, 2006 - ICU LOS between 14 and 28 days - Central access - 30 days to 18 years Exclusion Criteria: - Those who do not meet inclusion criteria |
Observational Model: Defined Population, Time Perspective: Longitudinal
Country | Name | City | State |
---|---|---|---|
United States | Children's Healthcare of Atlanta | Atlanta | Georgia |
Lead Sponsor | Collaborator |
---|---|
Children's Healthcare of Atlanta |
United States,
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