WithdrawnNCT03580005
Official study titleA Phase 4, Double-blind, Randomized, Parallel Group, Placebo-controlled Study Of The Efficacy And Safety Of Quillichew (Methylphenidate Hydrochloride (Hcl)) Extended Release Chewable Tablets (Erct) In 4-5 Year Old Children With Attention Deficit Hyperactivity Disorder (Adhd)
This study was withdrawn before enrollment.
Location not clearly listedADHDMedication studyAges 4–5
- Countries
- Sponsor
- Pfizer
CompletedNCT01933880
Official study titleAn Open, Self-Controlled, Prospective Study of Concerta on Cognitive Functions, Efficacy and Tolerance in the Pediatric Patients With Attention Deficit Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Multiple locations, including BeijingADHDMedication studyAges 7–12
- Countries
- China
- Sponsor
- Xian-Janssen Pharmaceutical Ltd.
CompletedNCT00700427
Official study titleMaintenance of Response After Open-Label Treatment With Atomoxetine Hydrochloride in Adult Outpatients With Attention-Deficit/Hyperactivity Disorder (ADHD): A Placebo-Controlled, Randomized Withdrawal Study
This study has finished and is no longer accepting participants.
Multiple locations, including ViennaADHDMedication studyAges 18–50
- Countries
- France, United Kingdom, Switzerland, + 9 others
- Sponsor
- Eli Lilly and Company
CompletedNCT03233867
Official study titleA Non-interventional Study to Identify Children and Adolescents (Ages 6-17 Years) With Attention Deficit Hyperactivity Disorder and With or Without Copy Number Variants in Specific Genes Involved in Glutamatergic Signaling and Neuronal Connectivity
This study has finished and is no longer accepting participants.
In WayneADHDObservational studyAges 6–17
- Countries
- United States
- Sponsor
- Aevi Genomic Medicine, LLC, a Cerecor company
CompletedNCT01886469
Official study titleA Phase II, Two-Stage, Open-Label, Single-Treatment, Adaptive Trial Design Examining the Pharmacokinetic and Pharmacodynamic Effects of up to Three Separate HLD100 Modified Release Formulations of Dextroamphetamine Sulfate in Adolescent (Stage 1) and Pediatric (Stage 2) Patients With Attention-Deficit Hyperactivity Disorder.
This study has finished and is no longer accepting participants.
In SaskatoonADHDMedication studyAges 6–17
- Countries
- Canada
- Sponsor
- Ironshore Pharmaceuticals and Development, Inc
CompletedNCT02086864
Official study titleA Randomized, Double Blind, Placebo Controlled Study of Homeopathic Treatment of Children and Youth With Attention Deficit Hyperactivity Disorder
This study has finished and is no longer accepting participants.
In TorontoADHDMedication studyAges 6–16
- Countries
- Canada
- Sponsor
- University of Toronto