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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00787085
Other study ID # 10024-05
Secondary ID NIH-AI01831
Status Completed
Phase N/A
First received November 6, 2008
Last updated November 6, 2008
Start date September 2001
Est. completion date February 2006

Study information

Verified date November 2008
Source Los Angeles Biomedical Research Institute
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Federal Government
Study type Observational

Clinical Trial Summary

This investigation is a epidemiologic case-control study of the risk factors associated with nosocomial funguria (fungi in the urine).


Description:

A recent large multi-center national surveillance survey of almost 5000 nosocomial (hospital based) urine isolates from medical intensive care units demonstrated that fungi comprised nearly 40% of urine isolates. Little is known about distinguishing fungi that cause colonization from those causing infection.

The objective of this study is to define the epidemiology of nosocomial funguria and natural history of patients that develop funguria while hospitalized.

Patients who may have eligible for this study will be identified from microbiology laboratory specimens at the Harbor-UCLA Medical Center and Cedars-Sinai Medical Center.


Recruitment information / eligibility

Status Completed
Enrollment 919
Est. completion date February 2006
Est. primary completion date February 2006
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients hospitalized at least 12 hours of any age (< 1 day to > 100 years of age) AND a urine or blood culture positive for fungi, OR urine culture negative for fungi (control group)

Exclusion Criteria:

- Patients already surveyed for funguria during current hospitalization and patients already being followed for recognized funguria

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States Cedars-Sinai Medical Center Los Angeles California
United States Harbor-UCLA Medical Center Torrance California

Sponsors (3)

Lead Sponsor Collaborator
Los Angeles Biomedical Research Institute Cedars-Sinai Medical Center, National Institute of Allergy and Infectious Diseases (NIAID)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Funguria Hospitalization day 0, 3, 7, 14, and every 7 days thereafter until hospital discharge or death No
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