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Monitoring of antibiotic treatment of patients with suspected sepsis using the biomarker Procalcitoni

Not Applicable
Conditions
Sepsis
C01.539.757
Registration Number
RBR-99h7tc
Lead Sponsor
niversidade Federal de Sergipe
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruitment completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Patients with suspected sepsis; hospitalized in critical areas (yellow, red clinic and ICU); Older than 18 years; Not pregnant.

Exclusion Criteria

Pregnancy discovered during collection; infections requiring prolonged antibiotic therapy, such as endocarditis, liver or brain abscess, deep abscess, mediastinitis and osteomyelitis; severe infection caused by viruses, parasites, fungi or mycobacteria; negative cultures (blood, urine, tracheal aspirate, or bronchoalveolar lavage) in patients with suspected sepsis, severe sepsis or septic shock.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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