Phase
Condition
Depression
Treatment
N/AClinical Study ID
Ages 15-24 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion:
Male or female subjects 15 years, 0 months - 24 years, 11 months of age at screening
For minor, at least one parent or step-parent/guardian with whom the subject lives is willing to participate in research sessions
For minor, the child and relative(s) are able and willing to give written informed assent/consent to participate, respectively
Subject has at least one first degree relative with Bipolar I Disorder, as assessed by the Structured Clinical Interview for DSM (SCID) or the Kiddie Schedule for Affective Disorders and Schizophrenia (KSADS-PL)
Subject shows evidence of current significant depressive symptoms as determined by a current Hamilton Depression Rating Scale (HAM-D) greater or equal to 8
Exclusion:
Patient has presence of current or lifetime history of manic or hypomanic mood episodes, psychotic disorders including schizophrenia, current major depressive episode, and/or more than two prior major depressive episodes
Patient has a DSM-5 diagnosis of autism, pervasive developmental disorder, OCD, PTSD, or Tourette's disorder
Patient has drug or alcohol abuse or dependence disorders in the three months prior to study recruitment, although a lifetime history of substance or alcohol disorders can be present if the patient has been abstinent for at least three months
Pregnancy; participants will be encouraged but not mandated to discuss a positive pregnancy test with their guardians (if minors) and we will follow local laws
Patient has history of major neurological disorders (such as epilepsy), or head trauma with > 10 minutes loss of consciousness
Patient has evidence of mental retardation (IQ less than 70), as determined by the Wechsler Abbreviated Scale of Intelligence (WASI)
Patient has any contraindication for MRI, including metal in the body related to an injury or surgery (e.g., surgical clips, metal fragments in the eyes), piercings that cannot be removed, or braces
Patient has history of allergic reaction to N-acetylcysteine
Study Design
Study Description
Connect with a study center
University of Cincinnati, Department of Psychiatry & Behavioral Neuroscience
Cincinnati, Ohio 45219
United StatesActive - Recruiting

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