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Pharmacogenetics of Antidepressant-Induced Disinhibition

Calgary, Alberta · Ages 6–17 · NCT03953014

The purpose of this study is to identify pharmacogenetic profiles associated with selective serotonin reuptake inhibitors (SSRI)-induced behavioral disinhibition in children with Major depressive disorder (MDD), anxiety disorders and/or obsessive-compulsive disorder (OCD) that could be used clinically to reduce the incidence of this adverse event and improve health outcomes.

Inclusion Criteria

1. Aged 6 - 24 years

2. Medical records available

3. Diagnosis of MDD, anxiety disorder, or OCD

4. Current or past history of SSRI therapy

Exclusion Criteria

1. Inability of parent/legal guardian to give informed consent

2. Inability of the child to give informed assent

3. Unwillingness of child to provide saliva sample for genetic analysis

4. Current, past or suspected diagnosis of attention deficit hyperactivity disorder, oppositional defiant disorder, conduct disorder, bipolar disorder, psychotic disorder, or pervasive developmental disorder.

View official listing on ClinicalTrials.gov ↗

This page is for general information only and is not a guarantee of eligibility or enrollment. Trial details are subject to change — the study site will confirm final eligibility criteria.