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Therapeutic regimens for brucellosis

Comparison of doxycycline-streptomycin, doxycycline-rifampin and ofloxacin-rifampin in the treatment of brucellosis: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT201101245681N1
Enrollment
191
Registered
2011-03-29
Start date
2008-04-21
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

Interventions

Intervention 1: doxycycline 200 mg/daily for six weeks plus streptomycin 1000mg/daily for the first three weeks. Intervention 2: ofloxacin 800 mg/daily plus rifampin 15 mg/kg daily for six weeks. Inte
Treatment - Drugs
doxycycline 200 mg/daily for six weeks plus streptomycin 1000mg/daily for the first three weeks
ofloxacin 800 mg/daily plus rifampin 15 mg/kg daily for six weeks
doxycycline 200 mg/daily plus rifampin 15 mg/kg daily for six weeks

Sponsors

Vice-Chancellor of Research and Technology,Hamedan University of Medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: clinical presentations compatible with brucellosis in the presence of significant titers of specific antibodies (standard tube agglutination = 1/160, coomb’s test = 1/160, 2-mercaptoetanol = 1-80, or Brucella IgG-ELISA > 12) and/or a positive blood culture for Brucella Exclusion criteria: age under 17 years, brucella endocarditis, neurobrucellosis, pregnancy, renal failure, hepatic failure, a history of treatment for brucellosis in the last six months

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Therapeutic failure. Timepoint: 6 weeks. Method of measurement: Physical examination.;Relapse. Timepoint: 6 months. Method of measurement: physical examination and 2-ME testing (2-ME>or=1/80).

Secondary

MeasureTime frame
Adverse reaction. Timepoint: 2, 4, 6 weeks. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Hamid Hashemi

Hamedan University of Medical sciences

hashemi@umsha.ac.ir+98 81 1827 4185

Outcome results

None listed

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