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Real-world evaluation of the efficacy of standardized treatment for Brucellosis

Real-world evaluation of the efficacy of standardized treatment for Brucellosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073276
Enrollment
Unknown
Registered
2023-07-05
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

brucellosis

Interventions

Acute phase - doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) for 6 weeks:None
Acute phase - doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) for 12 weeks:None
Chronic phase(complicated with osteoarthropathy) - doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) + ciprofloxacin (750mg bid) for 18 weeks:None
Chronic phase(complicated with osteoarthropathy) - doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) + ciprofloxacin (750mg bid) for 24weeks:None

Sponsors

The First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? To join the group voluntarily, able to understand and sign informed consent; ? According to the People's Republic of China health industry standards issued "brucellosis diagnosis" confirmed cases: acute, chronic (complicated with osteoarthrosis) brucellosis patients; (3) Willing and suitable to receive any of the following treatment options: Acute phase: Regimen 1: Doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) for 6 weeks; Regimen 2: Doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) for 12 weeks Chronic phase (complicated with osteoarthropathy) : Regimen 1: Doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) + ciprofloxacin (750mg bid) for 18 weeks; Regimen 2: Doxycycline (0.1g bid po) + rifampicin (10mg/kg qd) + ciprofloxacin (750mg bid) for 24 weeks;

Exclusion criteria

Exclusion criteria: ?A combination of other systemic diseases (including uncontrolled diabetes mellitus; Unstable coronary heart disease; Diseases of liver and kidney insufficiency; Malignant tumor; Ischemic/hemorrhagic stroke; Moderate to severe anemia; Parkinson's synthesis, etc.); ? Brucellosis patients with orchitis, meningitis, endocarditis, vasculitis and other complications; ? Mental illness with poor activity control, including delusions, hallucinations or suicidal ideation; ? Pregnant and lactating women; ? History of alcoholism, drug addiction or drug allergy;

Design outcomes

Primary

MeasureTime frame
Brucellosis titer;blood culture;Patient's clinical symptoms;

Secondary

MeasureTime frame
skin reaction factor;blood routine examination;complication;Biochemical blood;erythrocyte sedimentation rate (ESR);

Countries

China

Contacts

Public ContactLuXiaobo

The First Affiliated Hospital of Xinjiang Medical University

xjykdluxiaobo@126.com+86 159 9917 6213

Outcome results

None listed

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