Depression. Depressive episode In typical mild, moderate, or severe depressive episodes, the patient suffers from lowering of mood, reduction of energy, and decrease in activity. Capacity for enjoyment, interest, and concentration is reduced, and marked tiredness
Conditions
Interventions
Intervention 1: Intervention group: Patients in this group will take a SSIRs anti-dep ression medicine with Propolis (2000mg/70kg) during 6 weeks. Intervention 2: Control group: This group receives th
Sponsors
Academic Center for Education, Culture and Research (ACECR)
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Individuals with diagnosis of mild-moderate depression according HDRS score Age between 18-25 Outpatient Patients with no comorbid disorders diabetes, high blood pressure or cardiovascular disease Patients with no comorbid mental condition No consumption drugs other than SSRI Non-pregnant
Exclusion criteria
Exclusion criteria: Diagnosis of another non-depression disorder for patient during study Suicide inclination Taking anti depression medication except SSRI or electroconvulsive therapy impossibility to track disease (absence at the time of visit, cancellation of the continuation of the study and death) Occurrence of allergic reaction Occurrence of some side effect disorders such as fever, digestive and heart complications due to drug intake Hospitalization
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Formulation and primary sample. Timepoint: 6 months. Method of measurement: quantitative. | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical trials. Timepoint: 22th month. Method of measurement: questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAli Razmi
Academic Center for Education, Culture and Research (ACECR)
Outcome results
None listed