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Comparison between efficacy of ciprofioxacin - Doxycycline and rifampin – Doxycycline regimens in treatment of brucellosis

Comparison between efficacy of ciprofioxacin - Doxycycline and rifampin – Doxycycline regimens in treatment of brucellosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103146056N1
Enrollment
90
Registered
2012-03-10
Start date
2006-02-09
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Brucellosis. Brucellosis due to Brucella melitensis

Interventions

Treatment - Drugs
Intervention 1: In case group : ciprofloxacin 500mg twice aday and doycycline 100mg twice a day for two months. Intervention 2: In control group Rifampicin 300mg BID & Doxycyclin 100mg BID for two mou
In case group : ciprofloxacin 500mg twice aday and doycycline 100mg twice a day for two months
In control group Rifampicin 300mg BID & Doxycyclin 100mg BID for two mounths

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 76 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : patients with brucellosis in basis of clinical, epidemiological and serologic criteria, attended in the clinics of infectious disease in Arak university of medical sciences and age more than 17 years old. Excusion criteria : pregnancy; age less than 17 years; endocarditis - meningitis ; spondy lities, esophagitis ; consumption of oral contraceptives or phenytion; history of brucellosis (relapse), antimicrobial therapy for more than 7 days befor attending; intolerance for oral medication and no desire for patipicating.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical improvement. Timepoint: At the beginning of the study - second & third & and nine months serologic test in second & sixth& mounths. Method of measurement: Patients' history and physical exam and serologic results(clinical , wrigth , 2ME , serologic).

Secondary

MeasureTime frame
Failure of the treatment. Timepoint: Three mounth. Method of measurement: Clinical improvment and serology.;Drug side effects. Timepoint: During the treatment. Method of measurement: Clinical assessment.;Relapse. Timepoint: Sixth & ninth mounths from the begining of the study. Method of measurement: Clinical improvment and serology.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Farshideh Didgar

Arak University of Medical Sciences

dr.didgar@arakmu.ac.ir+98 86 1224 1411

Outcome results

None listed

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