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Cinnamomum tamala in the treatment of major depression

Evaluation of the efficacy of oral administration of Cinnamomum tamala with placebo in patients with depressive disorder

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171216037889N1
Enrollment
50
Registered
2018-01-22
Start date
2018-01-29
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

Depression. Major Depressive Disorder

Interventions

Intervention 1: Intervention group: cinnamomum tamala 250-500 mg daily plus sertraline 50-100 mg / day. Intervention 2: Control group: Placebo 250-500 mg daily with sertraline 50-100 mg / day.
Treatment - Drugs
Intervention group: cinnamomum tamala 250-500 mg daily plus sertraline 50-100 mg / day
Control group: Placebo 250-500 mg daily with sertraline 50-100 mg / day

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: presence of Major Depressive Disorder based on DSM-5 criteria baseline Hamilton Depression Rating Scale (HAM-D) (17-item) score of at least 18 18-60 years old

Exclusion criteria

Exclusion criteria: Exclusion criteria: presence of psychosis any other diagnosis in axis I and II; receiving psychotropic medications receiving any antidepressants during past one month or ECT during past two months; hypothyroidism cardiovascular problems pregnancy or nursing women

Design outcomes

Primary

MeasureTime frame
Depression score in Hamilton Test. Timepoint: 2,4,6. Method of measurement: Hamilton Depression Test.

Secondary

MeasureTime frame
Drug side effects. Timepoint: 1,2,4,6,Weeks. Method of measurement: Drug side effects questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaloumeh Ghaffari

Iran University of Medical Sciences

dr.salomehghafari@gmail.com+98 21 5515 2191

Outcome results

None listed

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