- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Conscience.
Displaying page 1 of 2.
| EudraCT Number: 2009-013283-39 | Sponsor Protocol Number: 2009-13 | Start Date*: 2009-10-07 |
| Sponsor Name:Assistance publique hôpitaux de marseille | ||
| Full Title: sevofluorane versus propofol pour l'intubation des nouveau-nés en réanimation | ||
| Medical condition: nouveau-nés en réanimation pédiatrique. | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005078-55 | Sponsor Protocol Number: N01183 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:UCB PHARMA | |||||||||||||
| Full Title: Named Patient Program with Levetiracetam Oral Solution, for Pediatric Patients suffering from Epilepsy having previously participated in study N01148 | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000869-11 | Sponsor Protocol Number: NC200601 | Start Date*: 2006-12-20 | |||||||||||
| Sponsor Name:Neuro-Consil GmbH | |||||||||||||
| Full Title: Comparison of efficacy and tolerability of rapid intravenous infusion of levetiracetam and sodium valproat. | |||||||||||||
| Medical condition: Focal epilepsy requiring rapid initiation of anticonvulsant protection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-000260-57 | Sponsor Protocol Number: ZNS-D-04-001 | Start Date*: 2005-04-25 | |||||||||||
| Sponsor Name:Eisai GmbH | |||||||||||||
| Full Title: Randomized trial to assess efficacy and safety of an add-on treatment with zonisamide in adults with focal epileptic seizures with or without secondary generalization | |||||||||||||
| Medical condition: Partial epileptic seizures with or without secondary generalisation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-006944-78 | Sponsor Protocol Number: 2006/0636 | Start Date*: 2007-05-11 |
| Sponsor Name:Centre Hospitalier Régional et Universitaire de Lille | ||
| Full Title: Evaluation du bénéfice de survie lors de l'adjonction de pentoxifylline à la corticothérapie dans l'hépatite alcoolique sévère | ||
| Medical condition: Etudier l'effet de l'adjonction de TORENTAL LP 400mg à la corticothérapie sur la survie à 6 mois des patients atteints d'Hépatite Alcoolique Sévère | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000421-31 | Sponsor Protocol Number: PHRC2012-02 | Start Date*: 2013-08-26 |
| Sponsor Name:CHU d'Angers | ||
| Full Title: Réversion préventive systématique versus réversion en cas d'hémorragie intracranienne chez les patients prenant un traitement antivitamine K et venant de subir un traumatisme cranien léger | ||
| Medical condition: hémorragies intracranienne | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-005440-25 | Sponsor Protocol Number: SP904 | Start Date*: 2009-02-16 | ||||||||||||||||
| Sponsor Name:UCB BIOSCIENCES, Inc. | ||||||||||||||||||
| Full Title: A Multicenter, Open-label Extension Trial to Assess the Long-term Use of Lacosamide Monotherapy and Safety of Lacosamide Monotherapy and Adjunctive Therapy in Subjects with Partial-onset Seizures | ||||||||||||||||||
| Medical condition: Partial-onset seizures (with and without secondary generalization) | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) IE (Completed) ES (Completed) AT (Completed) DK (Completed) PT (Not Authorised) IT (Completed) FR (Completed) DE (Completed) Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-017904-95 | Sponsor Protocol Number: P09-005 | Start Date*: 2010-06-28 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||||||||||||||||||||||
| Full Title: Open-Label Extension Study to Evaluate the Safety of USL255 as Adjunctive Therapy in Patients with Refractory Partial-Onset Seizures who had Participated in P09-004, a Randomized, Multicenter, Doub... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Refractory partial-onset seizures with or without secondary generalization | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) ES (Completed) GR (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2009-016996-31 | Sponsor Protocol Number: P09-004 | Start Date*: 2010-06-28 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Upsher-Smith Laboratories, Inc. | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Randomized, Multicenter, Double-Blind, Placebo–Controlled, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of USL255 as Adjunctive Therapy in Patients with Refractory Partial-O... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Refractory partial-onset seizures with or without secondary generalization | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) ES (Completed) GR (Completed) HU (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-002541-21 | Sponsor Protocol Number: NTL_CAP_07 | Start Date*: 2007-07-26 | |||||||||||
| Sponsor Name:NUTRIALYS | |||||||||||||
| Full Title: Etude de tolérance d'une association d'un aliment diététique destiné à une fin médicale spéciale caractérisé par une faible teneur en polyamines et une chimiothérapie par docetaxel chez des patient... | |||||||||||||
| Medical condition: patients volontaires atteints d'un adenocarcinome de la prostate métastatique et symptomatique en échappement hormonal | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001671-36 | Sponsor Protocol Number: EC11-103 | Start Date*: 2012-08-27 |
| Sponsor Name:Fundación para la Investigación Biomédica | ||
| Full Title: A phase IV randomized, controlled clinical trial to compare the high flow oxygen therapy (group of intervention) opposite to the conventional oxygen therapy (group control) in patients with severe ... | ||
| Medical condition: Severe acute respiratory failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-002929-78 | Sponsor Protocol Number: CARISEPY3007- Amendment INT-2/GBR-1 | Start Date*: 2007-11-13 | |||||||||||
| Sponsor Name:Ortho-McNeil Janssen Scientific Affairs, LLC | |||||||||||||
| Full Title: A Randomized, Double-blind, Parallel-group, Multicenter Study to Evaluate the Retention Rate, Efficacy, Safety, and Tolerability of Carisbamate, Topiramate and Levetiracetam as Adjunctive Therapy i... | |||||||||||||
| Medical condition: Partial onset seizures | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) CZ (Prematurely Ended) BE (Completed) FI (Completed) FR (Completed) IT (Prematurely Ended) ES (Completed) PT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005439-27 | Sponsor Protocol Number: SP902 | Start Date*: 2009-02-16 | ||||||||||||||||
| Sponsor Name:UCB BIOSCIENCES, Inc. | ||||||||||||||||||
| Full Title: A Historical-controlled, Multicenter, Double-blind, Randomized Trial to Assess the Efficacy and Safety of Conversion to Lacosamide 400mg/day Monotherapy in Subjects with Partial-onset Seizures | ||||||||||||||||||
| Medical condition: Partial-onset seizures (with or without secondary generalization) | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) IE (Completed) ES (Completed) AT (Completed) DK (Completed) PT (Not Authorised) IT (Completed) FR (Completed) DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-012919-17 | Sponsor Protocol Number: P071220 | Start Date*: 2009-11-12 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Etude multicentrique randomisée en double insu des effets de l'administration de norfloxacine ou d'un placebo sur la survie des malades atteints de cirrhose avec une insuffisance hépatocellulaire | |||||||||||||
| Medical condition: Malades atteints de cirrhose avec une insuffisance hépatocellulaire de grade C de Child-Pugh | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-013476-53 | Sponsor Protocol Number: PHRC-N/2009/POK-01 | Start Date*: 2010-09-02 |
| Sponsor Name:CHU de Nîmes | ||
| Full Title: Evaluation des performances de l’imagerie cérébrale isotopique du métabolisme glucidique en TEP (18F-FDG) et de la perfusion en TEMP (99mTc-ECD) pour le diagnostic de maladie d’Alzheimer au stade p... | ||
| Medical condition: Maladie d'alzheimer au stade prodromal | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-015632-15 | Sponsor Protocol Number: P071244 | Start Date*: 2010-01-22 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Essai en double aveugle contre placebo d'un traitement par inhibiteur de l'acétyl cholinesterase sur l'évolution d'un syndrome confusionnel chez les plus de 75 ans et évolution vers un syndrome dém... | |||||||||||||
| Medical condition: Syndrome confusionnel chez les personnes âgées de plus de 75 ans | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017081-23 | Sponsor Protocol Number: CPRC2009 - OPTIMA CC | Start Date*: 2010-03-22 | |||||||||||
| Sponsor Name:Centre Hospitalier Universitaire de Nancy | |||||||||||||
| Full Title: Optimisation du traitement du choc cardiogénique. Etude pilote physiopathologique ouverte multicentrique comparant l’efficacité et la tolérance de l’adrénaline et la noradrénaline (Optima CC) | |||||||||||||
| Medical condition: choc cardiogénique | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005782-35 | Sponsor Protocol Number: P070704 | Start Date*: 2008-04-23 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Efficacité du levetiracetam intra-veineux en association avec le clonazepam versus clonazepam seul dans la prise en charge pré-hospitalière de l'état de mal épileptique généralisé tonico-clonique | |||||||||||||
| Medical condition: Patient faisant un EMTC et pris en charge par une équipe du SMUR | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005731-67 | Sponsor Protocol Number: NLxxxxxxxxxx | Start Date*: 2021-07-02 | |||||||||||
| Sponsor Name:Haaglanden Medisch Centrum | |||||||||||||
| Full Title: Complement Inhibition: Attacking the Overshooting Inflammation @fter Subarachnoid Hemorrhage - A phase II trial on the safety and efficacy of C1 esterase inhibitor for the acute management of subar... | |||||||||||||
| Medical condition: Subarachnoid hemorrhage | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001453-31 | Sponsor Protocol Number: CONMED3 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Copenhagen University Hospital Rigshospitalet | ||||||||||||||||||
| Full Title: Automated pupillometry and NIRS-EEG to detect signatures of consciousness in acute brain injury after apomorphine and methylphenidate stimulation: A placebo-controlled, randomized, cross-over study | ||||||||||||||||||
| Medical condition: We investigate the possible effects of commercially available apomorphine and methylphenidate on signatures of consciousness in patients admitted to the ICU with acute disorder of consciousness, us... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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