Skip to content

celecoxib in the treatment of depressed patients with brucellosis

Celecoxib in the treatment of depression in patients with Brucellosis: a double blind randomized trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201405271556N59
Enrollment
50
Registered
2014-05-29
Start date
2014-06-22
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

Major depressive disorder. Major Depressive episode

Interventions

Intervention 1: Capsule Rifampine(900 mg/day in individuals with 75 kg weight or more and 600 mg/day in individuals with weight less than 75 kg)+ Cap. Doxycycline(100 mg bid)+ cap. celecoxib(200 mg bi
Treatment - Drugs
Placebo
Capsule Rifampine(900 mg/day in individuals with 75 kg weight or more and 600 mg/day in individuals with weight less than 75 kg)+ Cap. Doxycycline(100 mg bid)+ cap. celecoxib(200 mg bid) for 8 weeks
Capsule Rifampine(900 mg/day in individuals with 75 kg weight or more and 600 mg/day in individuals with weight less than 75 kg)+ Cap. Doxycycline(100 mg bid)+ cap. placebo for 8 weeks

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-Confirmation of brucellusis, 2age between 18 to 50 years old, 3- score lower than 20 in Hamilton Rating Scale for depression 4-Mild to moderate major depressive disorder based on DSM-V Exclusion criteria: 1-duration of brucellosis more than 3 months, 2-presence of localized brucellosis(including endocarditis, osteomyelitis), 3-psychotic disorder, 4-receiving psychotropic medications, 5-receiving antidepressants during the last month 6-receiving antibiotics during the last month, 7-patients who are under treatment with immunosuppressives, 8-history of cardiovascular disease, 9-pregnancy, 10-nursing women, 11-any significant medical condition(including malignancy, HIV infection, autoimmune disease,renal failure,hepatic failure), 12- other infectious diseases

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: Baseline and weeks 2-4-8 after beginig of treatment. Method of measurement: by Hamiltion Depression Rating Scale 17-Item.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactProf. Shahin Akhondzadeh

Tehran University of Medical Sciences

s.akhond@sina.tums.ac.ir+98 21 5541 2222

Outcome results

None listed

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