- 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 2 of 17.
EudraCT Number: 2020-005633-33 | Sponsor Protocol Number: 202000842 | Start Date*: 2021-06-02 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Prediction of ECT treatment response and reduction of Cognitive Side-effects using EEG and Rivastigmine | ||
Medical condition: A depressive disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006486-38 | Sponsor Protocol Number: ComplexitDOC_PSI | Start Date*: 2022-08-17 |
Sponsor Name:University of Liege | ||
Full Title: Complexity-enhancing drugs to treat disorders of consciousness (DoC): a psilocybin study | ||
Medical condition: Disorders of consciousness as unresponsive wakefulness syndrome (UWS) and minimally conscious state (MCS) after a coma due to acquired brain injury. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000791-26 | Sponsor Protocol Number: PHRI13-GF/LEVNEONAT-1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CHRU TOURS | |||||||||||||
Full Title: Lévétiracétam pour le traitement en première intention des convulsions du nouveau-né : étude de phase II | |||||||||||||
Medical condition: Nouveau-nés à terme présentant des convulsions dans les premières 72h de vie. Nés dans un contexte d'asphyxie périnatale qu'ils soient éligibles ou non à l'hypothermie thérapeutique. | |||||||||||||
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Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023668-42 | Sponsor Protocol Number: CRI 102194 | Start Date*: 2011-02-03 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Southampton University Hospital NHS Trust | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Pulmonary surfactant (S) biology in ventilated children on a paediatric intensive care unit with acute (A) hypoxic respiratory (R) failure- a pilot (P) study (S): (SARPS) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: acute hypoxic respiratory failure in children ventilated on paediatric intensive care | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003015-26 | Sponsor Protocol Number: AMZ002-002 | Start Date*: 2022-04-12 | |||||||||||||||||||||
Sponsor Name:Amzell B.V. | |||||||||||||||||||||||
Full Title: A Phase 3, Randomized, Open-Label Study to Evaluate the Efficacy and Safety of AMZ002, Compared to Vigabatrin, in the Treatment of Infantile Spasms | |||||||||||||||||||||||
Medical condition: Monotherapy for the treatment of infantile spasms (IS) in infants and children 2 months to 24 months of age | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) FR (Ongoing) PL (Prematurely Ended) IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001373-33 | Sponsor Protocol Number: 2016-3 | Start Date*: 2017-02-17 |
Sponsor Name:Region Ostergotland | ||
Full Title: Clinical Study Protocol An open phase IV,RCT, evaluating patient controlled sedation, in three different dosages of propofol in healthy subjects undergoing elective gynaecological out-patient su... | ||
Medical condition: Gynecological outpatient surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001491-21 | Sponsor Protocol Number: 1-2006 | Start Date*: Information not available in EudraCT |
Sponsor Name:Max Planck Institute of Psychiatry | ||
Full Title: Studies on Permeability of the Blood-Brain-Barrier for Escitaloprame related to various Genotypes of the ABCB1-Gene: Effects on Sleep and Motoric Learning | ||
Medical condition: Effects on sleep electroencephalogram and motoric learning in healthy volunteers related to the permeability of the blood-brain-barrier related to genotypes of the ABCB 1 gene | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001611-20 | Sponsor Protocol Number: 357-0-0 | Start Date*: 2018-07-24 |
Sponsor Name:University of Tübingen | ||
Full Title: Pathophysiology-based therapy of epileptic encephalopathies | ||
Medical condition: patients with epileptic encephalopathies | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-016907-41 | Sponsor Protocol Number: fMRT-Nociception | Start Date*: 2012-09-10 |
Sponsor Name:Charité, Universitätsmedizin Berlin | ||
Full Title: Investigation of nociceptive and antinociceptive mechanisms under anesthesia using fMRI, EEG and noxious reflexes | ||
Medical condition: This is a CT including only healthy volunteers. The aim of the study is to investigate the effect of a commonly used anesthetic drug in clinical concentrations on nociceptive and antinociceptive me... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003331-10 | Sponsor Protocol Number: HC03 | Start Date*: 2017-10-16 |
Sponsor Name:Leiden University | ||
Full Title: Acute effects of 40 mg cortisol on emotion and cognition. | ||
Medical condition: None. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002070-23 | Sponsor Protocol Number: EEGrofl | Start Date*: 2011-10-12 |
Sponsor Name:Maastricht University Medical Center | ||
Full Title: Effects of roflumilast on cognition in healthy adults: a behaviour-EEG study | ||
Medical condition: None; this proof-of-principle study will examine the cognition enhancing effects of roflumilast in healthy subjects | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000185-59 | Sponsor Protocol Number: 12012015 | Start Date*: 2015-03-03 | |||||||||||
Sponsor Name:Merja Kokki | |||||||||||||
Full Title: The effect of oxycodone to placental and fetal circulation during the phase I of labor and the efficacy, safety and neonatal effects of oxycodone. | |||||||||||||
Medical condition: Labor pain at the onset of labor in previously healthy women with normal pregnancy | |||||||||||||
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Population Age: In utero, Newborns, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010916-14 | Sponsor Protocol Number: 170209 | Start Date*: 2009-03-31 |
Sponsor Name:Antti Aho | ||
Full Title: Sugammadeksin vaikutus anestesiasyvyyden mittaamiseen | ||
Medical condition: Healthy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005571-10 | Sponsor Protocol Number: 03-08-21-12 | Start Date*: Information not available in EudraCT |
Sponsor Name:Kennedy Krieger Inst. Johns Hopkins Medicine | ||
Full Title: DEXTROMETORPHAN IN RETT SYNDROME | ||
Medical condition: Rett syndrome (RTT) is a neurological disorder with devastating consequences on the brain. It is characterized by stagnation of development followed by regression, both occurring between age 6 mont... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001098-13 | Sponsor Protocol Number: NA | Start Date*: 2008-04-30 |
Sponsor Name:UZ Leuven | ||
Full Title: Simultaneous administration of lorazepam and levetiracetam in non-convulsive status epilepticus, followed by IV valproate: a prospective, randomized, placebo-controled, double-blind pilot trial. | ||
Medical condition: Non-convulsive status epilepticus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004750-28 | Sponsor Protocol Number: PropoCon-Pilot | Start Date*: 2021-04-30 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Electrocardiographic And Clinical Effects Of Target-Controlled Infusion Of Propofol In Adults With Brugada Syndrome. A Pilot Study. | ||
Medical condition: Target Controlled Infusion of Propofol in patients with Brugada Syndrome. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003151-36 | Sponsor Protocol Number: AGO/2007/006 | Start Date*: 2007-08-01 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Sevoflurane-Remifentanil interaction: Multiple response surfaces, validation of calibration stimuli, validation of the intraoperative isobole concept and investigating remifentanil induced opioid t... | ||
Medical condition: American Society of Anesthesia class I and II patients scheduled for surgery under general anesthesia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003071-11 | Sponsor Protocol Number: AGO/2011/004 | Start Date*: 2012-02-17 |
Sponsor Name:Ghent University | ||
Full Title: Cognitieve en emotionele controle: gelijkenissen en verschillen in neuraal substraat - 11C-Raclopride | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013796-22 | Sponsor Protocol Number: NEU-2009-01 | Start Date*: 2009-11-23 | |||||||||||
Sponsor Name:Servicio de Neurología. Hospital Universitari de Bellvitge. | |||||||||||||
Full Title: Estatus epilépticos refractarios: utilidad de la monitorización de niveles plasmáticos. | |||||||||||||
Medical condition: Estatus epiléptico | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006487-30 | Sponsor Protocol Number: 150662 | Start Date*: 2009-09-11 | |||||||||||
Sponsor Name:St. James's Hospital | |||||||||||||
Full Title: Differential Effects of donepezil and placebo in mild cognitive impairment and elderly controls. | |||||||||||||
Medical condition: Amnestic Mild Cognitive Impairment (aMCI) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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