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New regimen of therapy in the treatment of human Brucellosis

Pre and post treatment level of Regulatory T cells in Brucellosis patients received Gentamicin and Doxycycline with levamisole

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014042617430N1
Enrollment
60
Registered
2014-05-12
Start date
2014-05-22
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

Intervention 1: Control group :Adminisration Gentamicin 4-5 mg / kg (IM) for a week, Doxcycycline 100 mg/bid (oral) for 45 days. Intervention 2: Intervention group: Adminisration Gentamicin 4-5 mg
Treatment - Drugs
Control group :Adminisration Gentamicin 4-5 mg / kg (IM) for a week, Doxcycycline 100 mg/bid (oral) for 45 days
Intervention group: Adminisration Gentamicin 4-5 mg / kg (IM) for a week, Doxcycycline 100 mg/bid ( oral) for 45 days and levamisole 80 mg( oral )daily for 6 weeks.

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 139 Years

Inclusion criteria

Inclusion criteria: After providing adequate information eligible patients volenteer will be enrolled in the study. Inclusion criteria: the patient had not received treatment, and also clinical signs and para clinical signs including, blood cultures, Wright test, 2ME and combs wright. Exclusion criteria: pregnant women; children younger than 8 years old; endocarditis, meningitis and spondylitis patients.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quantity of regulatory T cells. Timepoint: Before treatment,6 weeks after begining of treatment,6months after end of treatment. Method of measurement: Flow cytometric.;Brucella bacteria. Timepoint: Before treatment,6 weeks after begining of treatment,6months after end of treatment. Method of measurement: Blood culture.;??Antibody of serum. Timepoint: Before treatment,6 weeks after begining of treatment,6months after end of treatment. Method of measurement: Wright test,2ME,Coombs.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Hasanjani Roshan

Babol University of Medical Sciences

hagar2q@yahoo.ca drsoheil1503@yahoo.com+98 11 1220 7918

Outcome results

None listed

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