drugset / Trial / NCT02553161

Mechanism of Antidepressant-Related Dysfunctional Arousal in High-Risk Youth

NCT02553161

RandomizedParallel-groupTriple-blindTreatment

Summary

A 16-week double blind, placebo-controlled investigation of escitalopram in adolescents with depression and/or anxiety with a family history of Bipolar Disorder. Subjects will be evaluated using semi-structured diagnostic interviews and symptom ratings, participate in a MRI scan and then randomized to treatment. Following randomization, high-risk youth will have visits every week for the first 4 weeks of treatment then biweekly up to 16 weeks during which time tolerability and ratings will be performed. MRI scan will be repeated at week 4.

Timeline

Start
2015-12
Primary completion
2022-07
Completion
2022-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Escitalopram Small molecule 20 mg
Subject Escitalopram Small molecule 30 mg