TerminatedNCT01127646
Official study titleAssessing the Effect of Missing Doses (Off-Days) of Daily Medication in Patients Stable on Pharmacotherapy for ADHD Receiving Atomoxetine or OROS Methylphenidate: A Parallel Matched Group Clinical Study (On/Off Study)
This study ended early.
Multiple locations, including ArnhemADHDMedication studyAges 6–16
- Countries
- Netherlands, Spain, Sweden
- Sponsor
- Eli Lilly and Company
CompletedNCT00564954
Official study titleA Randomized, Multi-center, Double-blind, Cross-over Study Comparing the Efficacy and Safety of Focalin® XR 20 mg Versus Placebo at the 0.5 Hour Timepoint (Post-dose) in Children (6-12 Years) With Attention-Deficit/Hyperactivity Disorder (ADHD) in a Laboratory Classroom Setting
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 6–12
- Countries
- United States
- Sponsor
- Novartis Pharmaceuticals
CompletedNCT00922636
What is this study about?Researchers compared LY2216684, methylphenidate and placebo to find out how the approaches affected ADHD symptoms in children with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Spring ValleyADHDMedication studyAges 6–17
- Countries
- United States, Canada
- Sponsor
- Eli Lilly and Company
CompletedNCT00880217
What is this study about?Researchers compared JNJ-31001074 1 mg/d, JNJ-31001074 3 mg/d, JNJ-31001074 10 mg/d, Atomoxetine 80 mg/d, OROS methylphenidate HCl 54 mg/d and placebo to find out how the approaches affected ADHD symptoms in adults with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00890292
What is this study about?This study evaluated the safety of JNJ-31001074 for people with ADHD.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 12–17
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT00890240
What is this study about?This study evaluated the safety of JNJ-31001074 for people with ADHD.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–11
- Countries
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
CompletedNCT07001475
Official study titleA Phase Ib, Multicentre, Randomised, Double Blind, Placebo Controlled, 2 Sequence Crossover Trial to Evaluate the Effects of BI 3031185 on Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics in Patients With Borderline Personality Disorder or Attention-deficit/Hyperactivity Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including BerlinPersonality disorders, ADHDMedication studyAges 18–45
- Countries
- Germany
- Sponsor
- Boehringer Ingelheim
CompletedNCT05588713
Official study titleA Systematic Study of ADHD Assessments Within Child and Adolescent Psychiatric Care
This study has finished and is no longer accepting participants.
In UppsalaADHDInterventional studyAges 8–17
- Countries
- Sweden
- Sponsor
- Uppsala University
CompletedNCT05279313
What is this study about?Researchers studied Centanafadine Hydrochloride, tracking side effects to assess long-term safety and tolerability in children and adolescents with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including DothanADHDMedication studyAges 4–18
- Countries
- United States, Canada
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT00956605
Official study titleA Randomized Trial of Computer-based Attention-training Systems With and Without Neurofeedback in Children With ADHD
This study has finished and is no longer accepting participants.
In BostonADHDBehavioural studyAges 10–15
- Countries
- United States
- Sponsor
- Tufts Medical Center
CompletedNCT04786730
What is this study about?This study evaluated the safety of Centanafadine for people with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 4–12
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT04398225
What is this study about?This study evaluated the safety of Centanafadine for people with ADHD.
This study has finished and is no longer accepting participants.
In HollywoodADHDMedication studyAges 4–12
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)