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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180721040552N1
Enrollment
120
Registered
2019-04-04
Start date
2019-03-17
Completion date
Unknown
Last updated
2023-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystitis. Other cystitis

Interventions

Intervention 1: Intervention group: Every 12 hours, a supplement of 500 mg propolis and one 250 mg ciprofloxacin control. Intervention 2: Control group: Placebo and ciprofloxacin 250 mg every 12 hours

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: Alcohol use Chronic disease Taking antibiotics and other drugs

Design outcomes

Primary

MeasureTime frame
Urinary bacteria. Timepoint: At the beginning of the study and 7 days after the start of the study. Method of measurement: Urine culture.

Secondary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Shekari

Ghoum University of Medical Sciences

Mehdishekari025@gmail.com+98 25 3883 6354

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026