Health Condition 1: F332- Major depressive disorder, recurrent severe without psychotic features Health Condition 2: F331- Major depressive disorder, recurrent, moderate Health Condition 3: F321- Major depressive disorder, singleepisode, moderate Health Condition 4: F322- Major depressive disorder, singleepisode, severe without psychotic features
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Diagnosed with current Depressive episode according to ICD-11 (Single Episode Depressive Disorder / Recurrent Depressive Disorder)
Exclusion criteria
Exclusion criteria: 1)Diagnosed with current depressive episode in Bipolar affective disorder according to ICD-11 2)Presence of psychotic symptoms 3)Any contraindication to the use of Escitalopram or Buspirone 4)Any other co-morbid major psychiatric disorder(Except Tobacco dependence) 5)On current treatment for dementia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of combined Escitalopram (10 mg) and Buspirone (30 mg) vs Escitalopram (10 mg) monotherapy in improving cognition among elderly patients with Depression accompanied by cognitive impairment. Timepoint: Improvement in cognition and depressive symptoms will be measured at baseline, 4 weeks and 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To compare the efficacy of combined Escitalopram (10 mg) and Buspirone (30 mg) vs Escitalopram (10 mg) monotherapy in improving the depressive symptoms among elderly patients with Depression. 2)To compare the side-effect profile and drop-out from treatment in the combined Escitalopram and Buspirone group as compared with Escitalopram monotherapy group.Timepoint: 4 weeks and 8 weeks | — |
Countries
India
Contacts
Aiims, New Delhi