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Comparison of the therapeutic effect of ciprofloxacin and Combination of ciprofloxacin and propolis on women with cystitis

Phase 3
Conditions
Cystitis.
Other cystitis
N30.8
Registration Number
IRCT20180721040552N1
Lead Sponsor
Ghoum University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

Women with UTI (cystitis)
Age between 18 and 60 years
lower urinary tract infection for the first time

Exclusion Criteria

Alcohol use
Chronic disease
Taking antibiotics and other drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
rinary bacteria. Timepoint: At the beginning of the study and 7 days after the start of the study. Method of measurement: Urine culture.
Secondary Outcome Measures
NameTimeMethod
White blood cells. Timepoint: At the beginning of the study and 7 days after the start of the study. Method of measurement: Blood test.;Clinical symptoms. Timepoint: At the beginning of the study and 7 days after the start of the study. Method of measurement: Questionnaire.
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