Brucellosis. Brucellosis
Conditions
Interventions
Intervention 1: Intervention group: Receiver of Probiotic + Standard treatment of Brucellosis. Intervention 2: Control group: Receiver of Placebo + Standard treatment of Brucellosis.
Sponsors
Kashan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Having active brucellosis in the body Age between 18 to 60 years
Exclusion criteria
Exclusion criteria: having concurrent infections such as tuberculosis Not consuming probiotics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical Symptoms of Brucellosis include fever, sweating, fatigue, weight loss, joint pain, muscle pain, etc. Timepoint: baseline - 4weeks - 8weeks after starting intervention. Method of measurement: Questions to ask the patient about the clinical symptoms of brucellosis.;Laboratory criteria of Brucellosis. Timepoint: baseline - 4weeks - 8weeks after starting intervention. Method of measurement: Blood sampling and testing for Wright, Coombs Wright, 2ME, IgG, and IgM. | — |
Secondary
| Measure | Time frame |
|---|---|
| CRP (C-Reactive protein) and LFT. Timepoint: Baseline - 4 weeks - 8 weeks after intervention. Method of measurement: Blood sampling and testing for CRP, AST, ALT, AlkP. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyed Alireza Khatami Bidgoli
Kashan University of Medical Sciences
Outcome results
None listed