- Trials with a EudraCT protocol (66)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
66 result(s) found for: ADHD AND methylphenidate.
Displaying page 1 of 4.
| EudraCT Number: 2007-004664-46 | Sponsor Protocol Number: melmet | Start Date*: 2008-07-29 |
| Sponsor Name:No Sponsor | ||
| Full Title: Influence of methylphenidate on sleep and circadian rhythm in children with Attention-Deficit/Hyperactivity Disorder (ADHD) | ||
| Medical condition: Sleep disorders in Attention-Deficit/ Hyperactivity Disorder (ADHD) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000492-17 | Sponsor Protocol Number: NL39440.029.10 | Start Date*: 2012-10-29 |
| Sponsor Name:Afdeling Klinische Neuropsychologie Vrije Universiteit Amsterdam | ||
| Full Title: The Effects of Long-acting Methylphenidate on Academic Activity and Related Constructs in Children with ADHD: A Randomised Placebo Controlled Trial | ||
| Medical condition: Attention-deficit hyperactivity disorder (ADHD) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003660-11 | Sponsor Protocol Number: 74817 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Accare | ||
| Full Title: Do effects of methylphenidate decline after long-term use? A double-blind, placebo-controlled cross-over study of effects of methylphenidate on cognitive functioning and real world behavior in trea... | ||
| Medical condition: Attention Deficit Hyperactivity Disorder (ADHD) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-003285-26 | Sponsor Protocol Number: ASTA | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Universität Mainz, Klinik und Poliklinik für Kinder- und Jugendpsychiatrie und -psychotherapie | |||||||||||||
| Full Title: Effect of methylphenidate formulation on ADHD-patients' adherence to medical treatment. A comparison of Medikinet retard® (ER) once daily and Medikinet® (IR) twice daily in children and adolescents... | |||||||||||||
| Medical condition: Effect of methylphenidate formulation on ADHD-patients adherence to treatment | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002897-31 | Sponsor Protocol Number: 1453 | Start Date*: 2006-04-04 |
| Sponsor Name:North Bristol NHS Trust | ||
| Full Title: Objective assessment of attention difficulties in adults with Attention-Deficit Hyperactivity Disorder (ADHD) | ||
| Medical condition: Attention-Deficit Hyperactivity Disorder (ADHD) in Adults | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003888-59 | Sponsor Protocol Number: C.2524.0493.01 | Start Date*: 2014-03-17 |
| Sponsor Name:University of Amsterdam | ||
| Full Title: ADHD: Medication or Meditation? | ||
| Medical condition: Attention Deficit Hyperactivity Disorder (ADHD) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004053-76 | Sponsor Protocol Number: NL73102.018.20 | Start Date*: 2020-12-10 |
| Sponsor Name:Amsterdam UMC [...] | ||
| Full Title: Effectiveness of methylphenidate in children and adults with Smith Magenis syndrome and attention-deficit/hyperactivity disorder: An N-of-1 series | ||
| Medical condition: Smith Magenis syndrome | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004298-20 | Sponsor Protocol Number: MAMCAC02102014 | Start Date*: 2015-02-03 |
| Sponsor Name:Stockholm Centre for Dependency Disorders | ||
| Full Title: The effect of methylphenidate on executive functioning in amphetamine dependent individuals with ADHD | ||
| Medical condition: Amphetamine dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-012261-61 | Sponsor Protocol Number: 2009-4-CC | Start Date*: 2009-08-20 | ||||||||||||||||
| Sponsor Name:Academic Medical Center | ||||||||||||||||||
| Full Title: Why methylphenidate is not successful in cocaine-dependent ADHD patients: a SPECT study comparing DAT before and after methylphenidate treatment in ADHD patients with and without cocaine dependence | ||||||||||||||||||
| Medical condition: ADHD with and without substance use disorder (SUD) | ||||||||||||||||||
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| Population Age: Adults | Gender: Male | |||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-005017-12 | Sponsor Protocol Number: EyeADHD-01 | Start Date*: 2014-03-31 | |||||||||||
| Sponsor Name:Parnassia Bavo Groep - PsyQ | |||||||||||||
| Full Title: Looking into the eye of ADHD. Investigating the relationship between ADHD, the delayed circadian rhythm and the functioning of the eye. | |||||||||||||
| Medical condition: Adults with ADHD and suboptimal eye functioning. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000992-18 | Sponsor Protocol Number: 12-016 | Start Date*: 2014-09-26 |
| Sponsor Name:UMC Utrecht | ||
| Full Title: Proactive versus reactive inhibition in ADHD: Genetics, neurobiology and pharmacology | ||
| Medical condition: Attention-Deficit Hyperactivity Disorder (ADHD) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002249-35 | Sponsor Protocol Number: mkjf001 | Start Date*: 2006-10-26 |
| Sponsor Name:Addiction Center Stockholm | ||
| Full Title: Clinical trial of sustained release methylphenidate for Attention-Deficit-Hyperactivity-Disorder (ADHD) in adult criminal offenders with amphetamine addiction | ||
| Medical condition: 54 male prison inmates (27 in each treatment condition) that meet the DSM-IV criteria for amphetamine addiction and for ADHD and who are servicing their prison sentence are recruited. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-003049-13 | Sponsor Protocol Number: 7347 | Start Date*: 2022-08-24 |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: EEG-MRI study of the effect of methylphenidate on neural mechanisms in adult patients with ADHD with or without mood disorders: A randomized controlled trial versus placebo. | ||
| Medical condition: Attention Deficit Hyperactivity Disorder (ADHD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-004271-78 | Sponsor Protocol Number: CIAOII | Start Date*: 2016-05-31 | |||||||||||
| Sponsor Name:King's College London | |||||||||||||
| Full Title: Randomised controlled trial of the short term effects of OROS-methylphenidate on ADHD symptoms and behavioural outcomes in young male prisoners with attention deficit hyperactivity disorder | |||||||||||||
| Medical condition: Attention Deficit Hyperactivity Disorder (ADHD) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-002111-82 | Sponsor Protocol Number: 42603ATT3013 | Start Date*: 2007-10-24 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V., Turnhoutseweg 30, B-2340 Beerse, Belgium | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study to Evaluate Efficacy and Safety of Prolonged Release (PR) OROS® methylphenidate (54 and 72 mg/day) i... | |||||||||||||
| Medical condition: Attention Deficit-Hyperactivity Disorder (ADHD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) SE (Completed) NL (Completed) DK (Completed) FI (Completed) BE (Completed) GB (Completed) ES (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000488-15 | Sponsor Protocol Number: 3.0 | Start Date*: 2015-10-07 | |||||||||||
| Sponsor Name:University of Leipzig | |||||||||||||
| Full Title: Vigilance regulation as predictor of response to Psychostimulants in adult patients with ADHD | |||||||||||||
| Medical condition: Attention deficit-hyperactivity disorder | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004425-42 | Sponsor Protocol Number: CHDR0723 | Start Date*: 2008-09-15 | |||||||||||
| Sponsor Name:Centre for Human Drug Research | |||||||||||||
| Full Title: Neurocognitive testing in children with ADHD | |||||||||||||
| Medical condition: Attention Deficit Hyperactivity Disorder | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001174-29 | Sponsor Protocol Number: 77040 | Start Date*: 2021-05-31 |
| Sponsor Name:Amsterdam UMC | ||
| Full Title: Effectiveness of methylphenidate in adults with phenylketonuria and attention-deficit/hyperactivity disorder: An N-of-1 series | ||
| Medical condition: Phenylketonuria, ADHD | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000368-14 | Sponsor Protocol Number: NCA | Start Date*: 2017-12-14 |
| Sponsor Name:Sahlgrenska Univerisity Hospital Gothenburg | ||
| Full Title: A head-to-head randomized clinical trial of methylphenidate and lisdexamphetamine treatment for executive functions and global functioning in adults with ADHD | ||
| Medical condition: Attention Deficit Hyperactivity Disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002002-20 | Sponsor Protocol Number: 2014METAL1 | Start Date*: 2015-06-10 |
| Sponsor Name:UMCG | ||
| Full Title: A multicentre randomized double-blind placebo controlled discontinuation trial of methylphenidate | ||
| Medical condition: attention-deficit/hyperactivity disorder | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
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