Depression Clinical Trial
Official title:
A 12 Week Multi-Centre, Randomized, Double-Blind, Placebo Controlled Evaluation of the Most Efficacious and Tolerable Dose of Escitalopram in the Treatment of Elderly Patients
The study is designed to establish the efficacy and tolerability of escitalopram in the
treatment of depressive episodes of mild to moderate severity in the elderly.
The study is designed as a mainly naturalistic study including all patients of 65 years of
age or above that judged by the clinician would benefit from treatment by an antidepressant
medication. The study is designed as a double-blind, randomised placebo controlled study
with two groups of active treatment (escitalopram in two doses, 5 or 10 mg daily) in a
twelve week period.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
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