Effect of Mirtazapine on the quality of life of the breast cancer patients
Phase 3
Recruiting
- Conditions
- Condition 1: breast cancer. Condition 2: Major depressive disorder.Malignant neoplasm of breastMajor depressive disorder, single episode
- Registration Number
- IRCT20210425051075N1
- Lead Sponsor
- Sabzevar University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 110
Inclusion Criteria
Suffering from cancer
Major depressive disorder according to DSM IV criteria
Exclusion Criteria
Taking sleeping pills at the same time
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method