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Attention Deficit/Hyperactivity Disorder (ADHD - Pediatric) Clinical Trials

A listing of Attention Deficit/Hyperactivity Disorder (ADHD - Pediatric) medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (26) clinical trials

Study for Pediatric ADHD Learning that your [4 to 12] [4 or 5] year old child has attention-deficit/hyperactivity disorder (ADHD) is challenging. It may leave you wondering what options are available for your child and whether they will be safe for your child at such a young age. New clinical ...

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Is your child easily distracted? Is it hard for him to pay attention or wait his turn? Is it difficult for him to sit down to work without fidgeting or jumping up to do something else? Does he often act first and think later? Do these behaviors affect how he ...

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To evaluate the long-term safety and tolerability of flexibly-dosed dasotraline in children and adolescents w/ ADHD

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The purpose of this research study is to investigate brain changes in adolescents whoa re currently experiencing Attention Deficit Hyperactivity Disorder (ADHD) symptoms and have a family history of bipolar disorder. Participants will be randomized to mixed amphetamine salts or placebo for 12-week treatment.

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The purpose of this research study is to investigate brain changes in adolescents who are currently experiencing ADHD symptoms. Participants will be given mixed amphetamine salts for a 12-week treatment period.

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Does your child have ADHD? Meridien Research needs volunteers for a clinical study of a new medication for children with ADHD.

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If your child is experiencing any of the symptoms of ADHD, you may qualify to participate in a research study. Meridien Research is currently seeking individuals 6 to 12 years of age who have ADHD to participate in a research study. Please call 863-940-2087 for more information.

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The purpose of this research study is to investigate brain changes in adolescents who are currently experiencing depressive and/or anxiety symptoms and have a family history of bipolar disorder. Participants will be randomized to escitalopram and psychotherapy or placebo and psychotherapy for 16-week treatment.

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