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A Non-interventional Study to Identify Children and Adolescents With ADHD and With or Without mGLuR Mutations

Sponsored by Aevi Genomic Medicine, LLC, a Cerecor company

About this trial

Last updated 4 years ago

Study ID

AEVI-001-ADHD-002

Status

Completed

Type

Observational

Placebo

No

Accepting

18-75 Years
6 to 17 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 7 years ago

What is this trial about?

This is a non-interventional study in children and adolescents (ages 6-17 years) with attention deficit hyperactivity disorder (ADHD) to assess CNVs in specific genes involved in glutamatergic signaling and neuronal connectivity. The screening in this study will be conducted through a combination of online and site performed activities.

What are the participation requirements?

Yes

Inclusion Criteria

1. Parent/legally authorized representative (LAR) can speak and read English fluently, have provided informed consent and agree to be contacted for an interventional study prior to being genotyped.

2. Subject is 6 to 17 years of age (inclusive) at the time of informed consent.

3. Parent/LAR confirms that the subject has been diagnosed with or been told by a doctor that their child has ADHD.

4. Parent/LAR confirms that the subject is not pregnant and/or breastfeeding.

No

Exclusion Criteria

1. Parent/LAR confirms that the subject has been diagnosed with any of the following conditions (aside from ADHD): conduct disorder, anxiety disorder, major depression, autism spectrum disorder (ASD), bipolar disease, psychosis, hypertension, seizure disorder, syncope, or other serious cardiac problems.

2. Aside from your child's current ADHD medication (if applicable), parent/LAR confirms that the subject is currently taking any of the following medications: antidepressants, anti-anxiety medications, anti-psychotics, and/or mood stabilizers.

3. Parent/LAR confirms that the subject has been genotyped previously in the MDGN-NFC1-ADHD-001, MDGN-NFC1-ADHD-101 clinical study.