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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00900952
Other study ID # 3074X1-4489
Secondary ID
Status Completed
Phase N/A
First received May 7, 2009
Last updated October 8, 2009
Start date March 2009
Est. completion date June 2009

Study information

Verified date October 2009
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact n/a
Is FDA regulated No
Health authority Spain: Comité Ético de Investigación Clínica
Study type Observational

Clinical Trial Summary

The purpose of this observational study is to assess the prevalence and demographic and clinical characteristics of infections in elderly people admitted to Internal Medicine wards in Spain, as well as the etiology and resistance pattern for the main causal agents, and outcome.


Recruitment information / eligibility

Status Completed
Enrollment 240
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion criteria:

- Patients > 65 years of age that are hospitalized in an Internal Medicine ward and have an active infection (skin and soft tissue, intra-abdominal, or respiratory infections) from the community that needs antibiotic treatment

- Patients must have at least one sample processed for microbiological diagnosis

Exclusion criteria:

- COPD exacerbation

- Urinary tract infections

- Hospital acquired infections

- Other infections not in inclusion criteria

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Clinical record review


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wyeth is now a wholly owned subsidiary of Pfizer

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of each kind of infection will be measured from a descriptive point of view, using relative and absolute frequencies. 5 months No
Secondary Study the etiology and resistance pattern for the main causal agents. 5 months No
Secondary Describe the demographic features, co-morbidities, concomitant treatment and outcome of patients. 5 months No
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