Condition 1: breast cancer. Condition 2: Major depressive disorder. Malignant neoplasm of breast Major depressive disorder, single episode
Conditions
Interventions
Intervention 1: Intervention group: Patients will be treated with Mirtazapine 15-30 mg daily for 8 weeks. Intervention 2: Control group: Continuation of routine therapeutic care and no additional the
Sponsors
Sabzevar University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Suffering from cancer Major depressive disorder according to DSM IV criteria
Exclusion criteria
Exclusion criteria: Taking sleeping pills at the same time
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life. Timepoint: Study first and 8 weeks after starting mirtazapine. Method of measurement: WHO Quality of Life Questionnaire.;Anxiety. Timepoint: Study first and 8 weeks after starting mirtazapine. Method of measurement: WHO Quality of Life Questionnaire.;Sleep status. Timepoint: Study first and 8 weeks after starting mirtazapine. Method of measurement: WHO Quality of Life Questionnaire.;Appetite status. Timepoint: Study first and 8 weeks after starting mirtazapine. Method of measurement: WHO Quality of Life Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDanial Kamrani
Sabzevar University of Medical Sciences
Outcome results
None listed