- Trials with a EudraCT protocol (331)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
331 result(s) found for: EEG.
Displaying page 3 of 17.
| 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: 2012-001446-18 | Sponsor Protocol Number: SP0966 | Start Date*: 2014-02-11 | |||||||||||
| Sponsor Name:UCB Biosciences Inc. | |||||||||||||
| Full Title: A MULTI-CENTER, OPEN-LABEL, EXPLORATORY STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF LACOSAMIDE AS ADJUNCTIVE THERAPY IN SUBJECTS ≥1 MONTH TO <18 YEARS WITH EPILEPSY SYNDROMES ASSOCIATED WITH GE... | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) PL (Completed) Outside EU/EEA FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002750-24 | Sponsor Protocol Number: N01269 | Start Date*: 2021-04-16 |
| Sponsor Name:UCB Biopharma SRL | ||
| Full Title: A Randomized, Dose-Finding and Confirmatory, Double-Blind, Placebo-Controlled, Parallel-Group Multicenter Study With a 2-Stage Adaptive Design and Randomized Withdrawal to Evaluate the Efficacy, Sa... | ||
| Medical condition: Childhood absence epilepsy and juvenile absence epilepsy | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: PL (Completed) BE (Completed) IT (Trial now transitioned) SK (Trial now transitioned) Outside EU/EEA ES (Trial now transitioned) RO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004343-21 | Sponsor Protocol Number: LAM100036 | Start Date*: Information not available in EudraCT |
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||
| Full Title: A Multicenter, Double-Blind, Randomized, Parallel-group Evaluation of LAMICTAL Extended-release Adjunctive Therapy in Subjects with Primary Generalized Tonic-Clonic Seizures | ||
| Medical condition: Epilepsy - Primary genralised tonic clonic seizures | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-001496-21 | Sponsor Protocol Number: LOC-2013 | Start Date*: 2013-06-18 |
| Sponsor Name:Harry Scheinin | ||
| Full Title: The Neural Mechanisms of Anesthesia and Human Consciousness | ||
| Medical condition: No medical condition or disease involved. The study subjects are healthy volunteers. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-005651-41 | Sponsor Protocol Number: 2007-185 | Start Date*: 2008-01-24 | |||||||||||
| Sponsor Name:Peter Lommer Kristensen | |||||||||||||
| Full Title: Erythropoietins betydning for den kognitive funktion hos diabetikere under eksperimentel hypoglykæmi. | |||||||||||||
| Medical condition: Type 1 Diabetes / hypoglycaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001639-19 | Sponsor Protocol Number: 15-29900A | Start Date*: 2015-06-17 |
| Sponsor Name:Národní ústav duševního zdraví | ||
| Full Title: The efficacy of transcranial direct current stimulation (tDCS) in the treatment of depression and brain functional changes compared to venlafaxine. | ||
| Medical condition: Depressive disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004468-22 | Sponsor Protocol Number: HEAD-STUDIE | Start Date*: 2006-03-31 |
| Sponsor Name:Klinikum der Universität München, Kinderklinik und Poliklinik im Dr. von Haunerschen Kinderspital | ||
| Full Title: HEAD-TO-HEAD evaluation of the antiepileptic drugs Levetiracetam (LEV) vs. Sulthiame (STM) in a German multi-centre, doubleblind controlled trial in children with benign epilepsy with centro-tempor... | ||
| Medical condition: Benign epilepsy of childhood with centro-temporal spikes (BECTS) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-003369-50 | Sponsor Protocol Number: 200S14PF | Start Date*: 2015-03-03 |
| Sponsor Name:PASCOE pharmazeutische Präparate GmbH | ||
| Full Title: Proof of effectiveness of Pascoflair using qantitative measurement of electric brain activity during examination stress in 40 subjects suffering from test anxiety. A double-blind, randomized, plac... | ||
| Medical condition: Subjects who suffer from exam nerves | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004840-36 | Sponsor Protocol Number: CHDE-1 | Start Date*: 2015-09-03 |
| Sponsor Name:Hevert-Arzneimittel GmbH & Co. KG | ||
| Full Title: Proof of effectiveness of Calmvalera Hevert using qantitative measurement of electrical brain activity on 24 subjects during image and video-mediated cognitive and emotional stress. A double-blind,... | ||
| Medical condition: Subjects who suffer from exam nerves | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-004579-37 | Sponsor Protocol Number: MZ12-PCP-PalenicekTomas-A | Start Date*: 2014-06-18 |
| Sponsor Name:National Institute of Mental Health | ||
| Full Title: Animal and human serotonergic model of schizophrenia: validity evaluated by qEEG and fMRI | ||
| Medical condition: Inclusion criteria: a) Men and women at age between 28 and 65 years b) healthy volunteers with negative psychiatric history (severe mental illnesses that meet the criteria of ICD 10 F0.X - F99.X) ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-000788-27 | Sponsor Protocol Number: RD01273 | Start Date*: 2006-04-20 |
| Sponsor Name:Royal United Hospital Bath NHS Trust | ||
| Full Title: International Collaborative Infantile Spasms Study (ICISS) | ||
| Medical condition: Infantile spasms are a rare severe form of epilepsy affecting approx 1 in 2,250 infants, usually under the age of 1 year. Affected infants have a very abnormal EEG and a poor prognosis for subseque... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000436-41 | Sponsor Protocol Number: 2014-845 | Start Date*: 2015-07-24 | ||||||||||||||||
| Sponsor Name:Hospices Civils de Lyon | ||||||||||||||||||
| Full Title: Prévention des crises Epileptiques à la phase Aiguë des accidents vasculaires Cérébraux Hémorragiques | ||||||||||||||||||
| Medical condition: Haemorrhagic stroke | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-003651-30 | Sponsor Protocol Number: UCAB-CT-02 | Start Date*: 2016-12-01 |
| Sponsor Name:Umecrine Cognition AB | ||
| Full Title: Safety, tolerability and pharmacokinetics (PKs) of multiple oral doses of GR3027 in healthy male volunteers and single and multiple doses in patients with cirrhosis. Preliminary efficacy in cirrhot... | ||
| Medical condition: Hepatic encephalopathy (HE) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) DK (Completed) FI (Completed) PL (Completed) HU (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: 2013-003909-26 | Sponsor Protocol Number: BOP-TCI-001 | Start Date*: 2014-02-04 |
| Sponsor Name:UMCG | ||
| Full Title: Bayesian optimized Propofol Target-Controlled Infusion | ||
| Medical condition: Patients requiring general anaesthesia for surgery using propofol and requiring an arterial line for invasive blood pressure monitoring as part of their clinical care. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001551-11 | Sponsor Protocol Number: Iloprost | Start Date*: 2004-09-22 |
| Sponsor Name:Lund University Hospital | ||
| Full Title: Behandling av förhöjt pulmonellt arteriellt tryck med inhalerad iloprost | ||
| Medical condition: Nyfödda barn som är i behov av respiratorvård pga RDS, mekoniumaspiration eller primär lunghypertension | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003731-29 | Sponsor Protocol Number: WMTvsritalin | Start Date*: Information not available in EudraCT |
| Sponsor Name:SSE, Nevroklinikken, Oslo Universitetssykehus | ||
| Full Title: Could working memory training with computer games be an alternative to stimulant medication for children and adolescents with attention deficits and epilepsy? | ||
| Medical condition: Epilepsy and comorbid ADHD/ADD | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-001551-39 | Sponsor Protocol Number: 00003 | Start Date*: 2012-10-10 |
| Sponsor Name:Per H. Rosenberg | ||
| Full Title: Sitooko laskimoon annettu rasvaemulsio laskimoon annettua lidokaiinia? - farmakokineettinen ja neu-rofysiologinen tutkimus terveillä vapaaehtoisilla koehenkilöillä | ||
| Medical condition: Health volunteers used. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000070-29 | Sponsor Protocol Number: 74668 | Start Date*: 2022-09-15 |
| Sponsor Name:VU University Medical Center | ||
| Full Title: A Proof-of-Concept Study to Explore the Potential Efficacy of Deferiprone in Patients With Pelizaeus-Merzbacher disease (PMD) | ||
| Medical condition: Pelizaeus-Merzbacher disease | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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