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NCT00512772 Clinical Trial

Improved Use of Antibiotic Guidelines in Hospital Environment

Community-Acquired Pneumonia Clinical Trial

Official title:
Improved Use of Antibiotic Guidelines in in Hospital Environment: Research on an Implementation Model and the Role of the Hospital Pharmacist.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00512772
Other study ID # B32220072383
Secondary ID
Status Completed
Phase N/A
First received August 7, 2007
Last updated December 17, 2010
Start date October 2007
Est. completion date July 2010

Study information
Verified date July 2010
Source Katholieke Universiteit Leuven
Contact n/a
Is FDA regulated No
Health authority Belgium: Federal Agency for Medicinal Products and Health Products
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if the use of antibiotic guidelines and thus antibiotics can be improved through a description of possible barriers leading to tailored interventions.

Recruitment information / eligibility
Status Completed
Enrollment 823
Est. completion date July 2010
Est. primary completion date July 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Diagnosed community-acquired pneumonia (CAP)

- Diagnosed community-acquired pyelonephritis

Exclusion Criteria:

- CAP: hospital-acquired pneumonia; patients transferred from other hospital; death within 24h, aspiration pneumonia, immunocompromised status, palliative status, admission due to social reasons

- Pyelonephritis: urinary tract with functional or physical abnormalities, urinary catheterisation, pregnancy, (immunocompromised status, palliative status, admission due to social reasons and history of renal transplant.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Belgium Ziekenhuis Oost-Limburg Genk
Belgium Universitair Ziekenhuis Gasthuisberg Leuven

Sponsors (1)
Lead Sponsor Collaborator
Katholieke Universiteit Leuven

Country where clinical trial is conducted

Belgium, 

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