- Trials with a EudraCT protocol (369)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
369 result(s) found for: Neurological Disorder.
Displaying page 1 of 19.
| EudraCT Number: 2010-018627-25 | Sponsor Protocol Number: 68/2009 | Start Date*: 2010-02-25 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA MEYER | ||||||||||||||||||
| Full Title: PHARMACOLOGY STUDY FOR EFFICACY OF TOPIRAMATE ASSOCIATED WITH HYPOTHERIMIA TREATMENT IN NEWBORNS WITH HYPOXIC ISCHEMIC ENCEPHALOPATY: A PILOT STUDY | ||||||||||||||||||
| Medical condition: POST-ASPHYCTIC ENCEPHALOPATHY | ||||||||||||||||||
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| Population Age: Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-001185-91 | Sponsor Protocol Number: FMPS30094 | Start Date*: 2008-06-06 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
| Full Title: Central randomized, double-blind, crossover, multicenter clinical trial of Betametasone and placebo in children with ataxia teleangectasia | |||||||||||||
| Medical condition: ataxia teleangectasia | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000361-11 | Sponsor Protocol Number: RD639/24201 | Start Date*: 2006-06-23 | |||||||||||
| Sponsor Name:Fujimoto Pharmaceutical Corporation | |||||||||||||
| Full Title: A Proof of Concept Study to Determine the Minimum Effective Dose and to Assess the Efficacy and Safety of Subcutaneous Injections of FPFS-1169 in Parkinson's Disease Patients | |||||||||||||
| Medical condition: Treatment of Parkinson's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-005206-39 | Sponsor Protocol Number: deferiprone08 | Start Date*: 2008-10-13 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA OSPEDALI GALLIERA | |||||||||||||
| Full Title: Pilot Study: Iron-chelating treatment in patients with Neurodegeneration with Brain Iron Accumulation (NBIA). | |||||||||||||
| Medical condition: patients with NBIA | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-005749-30 | Sponsor Protocol Number: 2015-00887 | Start Date*: 2016-06-23 | |||||||||||
| Sponsor Name:Karolinska Institutet | |||||||||||||
| Full Title: A randomized, doubleblind, placebo-controlled multicenter trial to evaluate the safety and efficacy of rituximab (Mabthera) in subjects with new onset myasthenia gravis; the RINOMAX study | |||||||||||||
| Medical condition: New onset myasthenia gravis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003697-27 | Sponsor Protocol Number: CS2/713 | Start Date*: 2020-05-04 | |||||||||||
| Sponsor Name:AOU CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO | |||||||||||||
| Full Title: Effect of inhalatory sedation on cerebral perfusion in subarchnoid hemorrhage | |||||||||||||
| Medical condition: Patients with non traumatic subarachnoid hemorrhage (WFNS = 3 -5) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001039-23 | Sponsor Protocol Number: Alc 2006 - 01 | Start Date*: 2006-04-10 | |||||||||||
| Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
| Full Title: A Pilot Phase II Study for the evaluation of efficacy and tolerability of Gammaidroxybutyrate (ALCOVER) administered by oral route as add on treatmant in patients affected by DYT 11 Myoclonic Dysto... | |||||||||||||
| Medical condition: DYT 11 Myoclonic Dystonia. | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017160-17 | Sponsor Protocol Number: ALGO-01 | Start Date*: 2010-02-24 | ||||||||||||||||
| Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | ||||||||||||||||||
| Full Title: NSAID USED IN MESOTHERAPY VS NSAID INTRAMUSCOLAR INJECTION IN algodistrophy TREATMENT: A RANDOMIZED, CONTROLLED STUDY | ||||||||||||||||||
| Medical condition: SUFFERED FROM ALGODISTROPHY PATIENTS | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-012071-10 | Sponsor Protocol Number: 268/09 | Start Date*: 2009-06-15 | ||||||||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
| Full Title: Rivastigmine in the treatment of Sleep REM Behaviour Disorder (RBD) and Hallucinations in Parkinsonism: a Clinical and Polysomnographic study | ||||||||||||||||||
| Medical condition: PARKINSONISM | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-018056-42 | Sponsor Protocol Number: URC/2010/01 | Start Date*: 2010-07-09 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA G. BROTZU | |||||||||||||
| Full Title: A phase IV single-centre study to evaluate the topical administration of capsaicin cream (0.075%) as a healthy volunteer model of neuropathic pain. | |||||||||||||
| Medical condition: Creation of a healthy volunteer model of neuropathic pain. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002005-45 | Sponsor Protocol Number: OsmoBrain | Start Date*: 2007-05-11 | |||||||||||
| Sponsor Name:A.O. San Gerardo di Monza | |||||||||||||
| Full Title: Comparative trial between HyperHAES (7.2% sodio cloruro / 6% hydrxyethyl starch) and 20% mannitol for treatmenti intracranial hypertension in traumatic brain injury | |||||||||||||
| Medical condition: Brain trauma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-016066-91 | Sponsor Protocol Number: EPO200901 | Start Date*: 2010-03-10 | |||||||||||
| Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
| Full Title: SAFETY AND EFFICACY OF ERYTHROPOIETIN IN AMYOTROPHIC LATERAL SCLEROSIS: A RANDOMIZED, PLACEBO-CONTROLLED CLINICAL TRIAL | |||||||||||||
| Medical condition: ALS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-016684-11 | Sponsor Protocol Number: meloxicam09 | Start Date*: 2010-02-24 | |||||||||||
| Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | |||||||||||||
| Full Title: Meloxicam periradicular injection in physiological solution vs physiological solution in the treatment of lumbar and/or sacral radiculite: single blind randomized study | |||||||||||||
| Medical condition: patients with radiculite lumbar and/or sacral pain. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000770-60 | Sponsor Protocol Number: CFTY720DIT03 | Start Date*: 2011-04-12 | |||||||||||
| Sponsor Name:NOVARTIS FARMA | |||||||||||||
| Full Title: “An open-label, multi-center, expanded access study with fingolimod in patients with relapsing-remitting multiple sclerosis for whom no suitable therapy exists” | |||||||||||||
| Medical condition: approximately 600 patients with relapsing-remitting MS for whom no suitable therapy exists i.e. where existing therapies have failed. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001556-11 | Sponsor Protocol Number: 1058 | Start Date*: 2011-05-23 | ||||||||||||||||
| Sponsor Name:IRCCS FONDAZIONE STELLA MARIS | ||||||||||||||||||
| Full Title: Decline of mentale functions in adults with Down Syndrome: clinical and experimental study on the effects of treatment with fluoxetine and of cognitive and physical training. | ||||||||||||||||||
| Medical condition: Adults (over 30 years) with Down Syndrome. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-010661-23 | Sponsor Protocol Number: 2009-010661-23 | Start Date*: 2009-07-30 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA DELLA SECONDA UNIVERSITA` DEGLI STUDI DI NAPOLI | |||||||||||||
| Full Title: MITOXANTRONE/GLATIRAMER ACETATE COMBINED TREATMENT IN THE THERAPY OF SECONDARY-PROGRESSIVE MULTIPLE SCLEROSIS | |||||||||||||
| Medical condition: subjects affected by secondary-progressive Multiple Sclerosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004571-37 | Sponsor Protocol Number: AOBS-NEU-RPF-2011 | Start Date*: 2012-02-21 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: - Rescue of Progranulin HaploInsufficiency in Frontotemporal Dementia | |||||||||||||
| Medical condition: frontotemporal dementia associated to progranulin deficit | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-007162-32 | Sponsor Protocol Number: RMaIDSM | Start Date*: 2007-10-30 | |||||||||||
| Sponsor Name:ISTITUTO C. MONDINO | |||||||||||||
| Full Title: ADVANCED MRI STUDY ON INFLAMMATORY AND DEGENRATIVE DAMAGE IN MULTIPLE SCLEROSIS | |||||||||||||
| Medical condition: Multiple Sclerosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024270-19 | Sponsor Protocol Number: CCD-1014-PR-0053 | Start Date*: 2011-05-09 | |||||||||||
| Sponsor Name:CHIESI | |||||||||||||
| Full Title: A Randomized, Placebo-Controlled, Multicenter Study to Evaluate the Safety and Tolerability of Multiple Dose Regimens of CHF 5074 (200, 400, 600 mg/day for up to 12 Weeks) and to Explore the Eff... | |||||||||||||
| Medical condition: Mild Cognitive Impairment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001881-14 | Sponsor Protocol Number: GIFT/1 | Start Date*: 2013-03-01 | |||||||||||
| Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
| Full Title: A phase II clinical trial to evaluate the safety and efficacy of interferon gamma in elevating frataxin levels in Friedreich ataxia patients | |||||||||||||
| Medical condition: Friedreich's Ataxia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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