- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Spinal root.
Displaying page 1 of 1.
EudraCT Number: 2011-005684-24 | Sponsor Protocol Number: CME-LEM2 | Start Date*: 2014-01-16 | |||||||||||
Sponsor Name:Fundación Investigación Biomédica Hospital Universitario Puerta de Hierro | |||||||||||||
Full Title: Subarachnoid administration of autologous bone marrow stromal cells in incomplete spinal cord injury. | |||||||||||||
Medical condition: Incomplete spinal cord injury, due to traumatical or ischemic cause. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006938-94 | Sponsor Protocol Number: TRANEX2009 | Start Date*: 2010-03-18 | |||||||||||||||||||||
Sponsor Name:Dra Maria José Colomina Soler | |||||||||||||||||||||||
Full Title: Ensayo clínico multicéntrico, aleatorizado y controlado con placebo para evaluar la eficacia de la utilización perioperatoria de ácido tranexámico sobre la hemorragia quirúrgica en la cirugía compl... | |||||||||||||||||||||||
Medical condition: Prevención antihemorrágica en cirugia compleja de columna Antihemorragic prevention major spinal surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000321-41 | Sponsor Protocol Number: ALENDROHNP2011 | Start Date*: 2012-04-18 | |||||||||||
Sponsor Name:FUNDACION HOSPITAL NACIONAL DE PARAPLEJICOS PARA LA INVESTIGACIÓN Y LA INTEGRACIÓN | |||||||||||||
Full Title: PREVENTIVE TREATMENT OF BONE MASS LOSS WITH ALENDRONATE AND CALCIFEDIOL IN PATIENTS WITH ACUTE SPINAL CORD INJURY | |||||||||||||
Medical condition: Preventing loss of bone density in patients with spinal cord injury of traumatic etiology complete during the first year of evolution of the lesion. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002744-22 | Sponsor Protocol Number: 8040 | Start Date*: 2007-10-18 | |||||||||||
Sponsor Name:University Hospital of Montpellier | |||||||||||||
Full Title: Effet d'un traitement anti-résorptif sur la perte osseuse chez le patient blessé médullaire | |||||||||||||
Medical condition: patient blessé medullaire | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004373-80 | Sponsor Protocol Number: ASBI603 | Start Date*: 2013-06-21 | |||||||||||
Sponsor Name:Asubio Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of SUN13837 Injection in Adult Subjects with Acute Spinal Co... | |||||||||||||
Medical condition: Acute spinal cord injury | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006503-15 | Sponsor Protocol Number: STA-LDH01 | Start Date*: 2023-02-23 | |||||||||||||||||||||
Sponsor Name:Stayble Therapeutics | |||||||||||||||||||||||
Full Title: A prospective, randomised, double-blinded, placebo-controlled study investigating the safety and tolerability of STA363 in patients with radiculopathy caused by lumbar disc herniation | |||||||||||||||||||||||
Medical condition: Radiculopathy due to lumbar intervertebral disc herniation | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002948-10 | Sponsor Protocol Number: A0081007 | Start Date*: 2005-07-14 | |||||||||||
Sponsor Name:Pfizer AB | |||||||||||||
Full Title: A Randomised Placebo-Controlled Trial of the Efficacy and Safety of Pregabalin in the Treatment of Subjects with Neuropathic Pain Associated with Lumbo-sacral Radiculopathy (protocol dates 2004-11... | |||||||||||||
Medical condition: Pain associated with lumbo-sacral radiculopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001449-26 | Sponsor Protocol Number: 6603/1132 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Seikagaku Corporation | |||||||||||||
Full Title: A Multicenter, Open-label Study of SI-6603 in Patients with Lumbar Disc Herniation (Phase III) | |||||||||||||
Medical condition: Lumbar disc herniation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006176-30 | Sponsor Protocol Number: NW-1029/01-08 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:Newron Pharmaceuticals S.p.A. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF TWO FIXED DOSES (160 OR 320 MG/DAY) OF RALFINAMIDE IN PATIENTS WITH CHRONIC NEUROPATHIC LOW BACK PAIN. A MULTICENTER, DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED 12- WEEK ST... | |||||||||||||
Medical condition: Chronic neuropathic low back pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012836-33 | Sponsor Protocol Number: KIP113049 | Start Date*: 2009-11-26 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A randomised, double blind study to evaluate the safety and efficacy of the p38 kinase inhibitor, GW856553, in subjects with neuropathic pain from lumbosacral radiculopathy | |||||||||||||
Medical condition: Neuropathic pain from lumbosacral radiculopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) DK (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005506-32 | Sponsor Protocol Number: Dulo2006 | Start Date*: 2007-03-05 | |||||||||||
Sponsor Name:Danish Pain Research Center | |||||||||||||
Full Title: Pain, anxiety and depression in neuropathic and non-neuropathic pain: Effect of monoamine modulation. | |||||||||||||
Medical condition: Chronic pain: neuropathic pain and fibromyalgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005008-32 | Sponsor Protocol Number: ICORG13-17 | Start Date*: 2014-07-16 |
Sponsor Name:Cancer Trials Ireland | ||
Full Title: A phase II Study of the Efficacy and Safety of lenalidomide, subcutaneous bortezomib, and dexamethasone combination therapy for patients with newly diagnosed multiple myeloma | ||
Medical condition: Newly diagnosed multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015496-27 | Sponsor Protocol Number: Etoricox09-10 | Start Date*: 2010-03-15 | |||||||||||||||||||||||||||||||
Sponsor Name:BG university hospital Bergmannsheil GmbH | |||||||||||||||||||||||||||||||||
Full Title: Wirksamkeit von Etoricoxib bei Patienten mit neuropathischen Schmerzen mit und ohne peripherer Hyperalgesie (Efficacy of etoricoxibe in patients with neuropathic pain with and without peripheral hy... | |||||||||||||||||||||||||||||||||
Medical condition: Animal experiments analysing anti-hyperalgesic effects of Coxibs show inconsistent results due to different used dosages and varying different pain models. Theoretical the use of NSAIDs is rational... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004775-78 | Sponsor Protocol Number: 1014802-203 | Start Date*: 2016-05-09 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of BIIB074 in Subjects With Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
Medical condition: Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LV (Completed) GB (Completed) CZ (Completed) SK (Completed) AT (Completed) ES (Completed) NL (Completed) BE (Completed) FR (Completed) RO (Completed) BG (Completed) LT (Prematurely Ended) IT (Completed) | ||||||||||||||||||
Trial results: View results |
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