- Trials with a EudraCT protocol (374)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
374 result(s) found for: Neurologic disease.
Displaying page 1 of 19.
EudraCT Number: 2019-002473-65 | Sponsor Protocol Number: PET-PiB | Start Date*: 2021-06-16 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: PET-CT study of cerebral regional amyloid burden in Patients with suspected Alzheimer’s disease | |||||||||||||
Medical condition: Patients with amnestic or non-amnestic MCI or early dementia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2016-001955-29 | Sponsor Protocol Number: 024PKAN15004 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Retrophin, Inc. | |||||||||||||
Full Title: Efficacy, Safety, and Tolerability of Fosmetpantotenate (RE-024), a Phosphopantothenate replacement therapy, in patients with Pantothenate Kinase-associated Neurodegeneration (PKAN): A Randomized, ... | |||||||||||||
Medical condition: Pantothenate kinase associated neurodegeneration (PKAN), an autosomal recessive genetic disorder, the most common form of Neurodegeneration with Brain Iron Accumulation (NBIA). It is a progressive,... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) GB (Prematurely Ended) CZ (Prematurely Ended) NO (Completed) FR (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 2016-002160-14 | Sponsor Protocol Number: 20160516 | Start Date*: 2016-11-22 |
Sponsor Name:St. Antonius Hospital | ||
Full Title: 68Ga-DOTA-NOC PET/CT for the imaging of disease activity in neurologic and cardiac sarcoidosis. | ||
Medical condition: Sarcoidosis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005178-30 | Sponsor Protocol Number: LRS-01-07-02 | Start Date*: 2008-01-09 | |||||||||||||||||||||
Sponsor Name:Life Recovery Systems | |||||||||||||||||||||||
Full Title: Clinical Study of the LRS ThermoSuit™ System in Post Arrest Patients with Intravenous Infusion of Magnesium Sulfate | |||||||||||||||||||||||
Medical condition: Post resusucitation disease after resuscitation from cardiac arrest | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||||||||||||
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: 2014-001427-79 | Sponsor Protocol Number: TIRCON2012V1-EXT | Start Date*: 2015-03-27 |
Sponsor Name:ApoPharma Inc. | ||
Full Title: Long-term Safety and Efficacy Study of Deferiprone in Patients with Pantothenate Kinase-Associated Neurodegeneration (PKAN) | ||
Medical condition: Pantothenate kinase-associated neurodegeneration (PKAN) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) IT (Completed) | ||
Trial results: View results |
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) |
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: 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: 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: 2009-018056-42 | 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: 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: 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) |
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