None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 18-45 years of male and female, diagnosed as case of major depressive disorder, not been treated for the index episode.
Exclusion criteria
Exclusion criteria: Subjects with comorbid psychiatric disorder except for the comorbid anxiety symptoms and tobacco use, known case of diabetes or hypertension or dyslipidemia or hyperthyroidism, hypothyroidism, with medical or surgical condition that affect his or her locomotor capabilities, pregnancy and lactating female.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the efficacy, tolerability and metabolic parameters on subjects treated with vortioxetine versus escitalopram in the management of major depressive disorder.Timepoint: At baseline, week 4th and week 12th | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the treatment adverse effects responsible for intolerance of vortioxetine and escitalopram by using the anti depressant side effect checklist.Timepoint: Baseline, week 4, week 12.;To study the association of efficacy and tolerability of vortioxetine and escitalopram in the management of major depressive disorder.Timepoint: Baseline, week 4, week 12. | — |
Countries
India
Contacts
Eras lucknow medical college and hospital