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ew regimen of therapy in the treatment of human Brucellosis

Phase 2
Conditions
brucellosis.
Brucellosis due to Brucella melitensis
Registration Number
IRCT2014041217230N1
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
160
Inclusion Criteria

After providing adequate information eligible patients volenteer will be enrolled in the study.
Patients who have received no treatment,Clinical signs and positive Blood culture,positive serological tests such as Wright and 2ME and Coombs Wright.
Exclusion criteria : pregnant women and children less than 8 years, patients with endocarditis, meningitis or spondylitis , Negative PCR tests are also excluded

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
DNA of Brucella bacteria. Timepoint: Three sections: in first day of the study, end of the sixth week, end of the sixth month. Method of measurement: PCR.;Brucella bacteria. Timepoint: Three sections: in first day of the study, end of the sixth week, end of the sixth month. Method of measurement: Blood culture.;Antibody of serum. Timepoint: Before treatment, 6 weeks after begining of treatment, 6months after end of treatment. Method of measurement: Wright test, 2ME, Coombs.
Secondary Outcome Measures
NameTimeMethod
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