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Minocycline in the treatment of Depression

Minocycline in the treatment of mild to moderate depression in patients with HIV: A randomized placebo controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201405271556N57
Enrollment
50
Registered
2014-05-27
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: CapsuleMinocycline100 mg BID as intervention group for 6 weeks. Intervention 2: Cap. placebo as control group for 6 weeks.
Treatment - Drugs
Placebo
CapsuleMinocycline100 mg BID as intervention group for 6 weeks

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-Confirmation of HIV infection by Western-blot test 2-receiving HAART medications 3- score lower than 20 in Hamilton Rating Scale for depression 4-Mild to moderate major depressive disorder based on DSM-V 5-consent for entering the trial Exclusin criteria: 1-receving antidepressants, 2-ongoing addiction, 3-opportunistic infections during 45 days before entering the trial, 4-severe depression and suicidality, 6-death of loved ones during the last month, 7-active infection and fever, 8-cancer, 9-pregnancy, 10-alcohol dependence, 11-history of allergy to minocycline or other tetracyclines, 12- Cognitive disorders including dementia due to HIV

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of depression. Timepoint: Baseline and weeks 1-3-6 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