- Trials with a EudraCT protocol (458)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
458 result(s) found for: Peripheral Neuropathy.
Displaying page 2 of 23.
EudraCT Number: 2006-004545-42 | Sponsor Protocol Number: TRO19622 CLEQ 1104-1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:TROPHOS | |||||||||||||
Full Title: A double-blind, randomized, multi-center study with 500 mg QD of TRO19622 versus placebo in patients with painful peripheral diabetic neuropathy | |||||||||||||
Medical condition: Painful peripheral diabetic neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003656-38 | Sponsor Protocol Number: CRC 235 | Start Date*: 2006-11-08 | |||||||||||
Sponsor Name:University of Surrey Clinical Research Centre | |||||||||||||
Full Title: A Double-blind, Randomised, Parallel Groups Investigation into the Effects of Pregabalin, Duloxetine and Amitriptyline on Aspects of Pain, Sleep, and Next Day Performance in Patients Suffering from... | |||||||||||||
Medical condition: Diabetic Peripheral Neuropahty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004733-41 | Sponsor Protocol Number: A6061037 | Start Date*: 2008-03-14 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND PLACEBO CONTROLLED TRIAL OF [S,S]-REBOXETINE IN PATIENTS WITH CHRONIC PAINFUL DIABETIC PERIPHERAL NEUROPATHY | |||||||||||||
Medical condition: CHRONIC PAINFUL DIABETIC PERIPHERAL NEUROPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) FI (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005748-18 | Sponsor Protocol Number: SN07NE080 | Start Date*: 2009-01-02 | |||||||||||
Sponsor Name:Greater Glasgow and Clyde NHS Board and The University Of Glasgow | |||||||||||||
Full Title: SAFETY AND TOLERABILITY OF ECULIZUMAB IN THE TREATMENT OF MULTIFOCAL MOTOR NEUROPATHY: AN OPEN LABEL STUDY | |||||||||||||
Medical condition: Multifocal motor neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016457-18 | Sponsor Protocol Number: E05-CL-3001 | Start Date*: 2010-07-20 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd | |||||||||||||
Full Title: A Multicentre, Single-Arm, Open-Label Study Of The Repeated Administration Of QUTENZA For The Treatment Of Peripheral Neuropathic Pain | |||||||||||||
Medical condition: Peripheral Neuropathic Pain in Postherpetic Neuralgia (PHN), Painful HIV-Associated Neuropathy (HIV-AN), Peripheral Neuropathic Injury (PNI), Idiopathic Small Nerve Neuropathy (ISNN) or other Perip... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) FR (Completed) BE (Completed) GB (Completed) CZ (Completed) FI (Completed) ES (Completed) AT (Completed) IT (Completed) HU (Completed) NL (Completed) SK (Completed) PL (Completed) SI (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011254-18 | Sponsor Protocol Number: AEG33773-201 | Start Date*: 2009-10-02 | |||||||||||
Sponsor Name:Aegera Therapeutics Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Comparing the Safety and Efficacy of AEG33773 versus Placebo in Patients with Painful Diabetic Peripheral Neuropathy | |||||||||||||
Medical condition: Painful diabetic peripheral neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002743-10 | Sponsor Protocol Number: A0081268 | Start Date*: 2012-01-05 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A STUDY OF PREGABALIN IN THE TREATMENT OF SUBJECTS WITH PAINFUL DIABETIC PERIPHERAL NEUROPATHY WITH BACKGROUND TREATMENT OF NSAID FOR OTHER PAIN CONDITIONS | |||||||||||||
Medical condition: PAINFUL DIABETIC PERIPHERAL NEUROPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016458-42 | Sponsor Protocol Number: E05-CL-3002 | Start Date*: 2011-10-20 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Randomized, Controlled, Long-term Safety Study Evaluating the Effect of Repeated Applications of QUTENZA plus Standard of Care versus Standard of Care alone in Subjects with Painful Diabetic Peri... | |||||||||||||
Medical condition: Painful Diabetic Peripheral Neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) CZ (Completed) NL (Completed) ES (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002787-95 | Sponsor Protocol Number: WP-07-148 | Start Date*: 2008-01-03 | |||||||||||
Sponsor Name:Department of Pulmonology, Rijnstate Hospital | |||||||||||||
Full Title: A randomized double-blind study of N-Acetylcysteine vs. placebo to Prevent Neurotoxicity induced by Platinum containing chemotherapy in patients treated for (Non)Small Cell Lung Cancer and Malignan... | |||||||||||||
Medical condition: Cisplatin-induced peripheral neuropathy will be investigated. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002827-14 | Sponsor Protocol Number: TreatSPG11 | Start Date*: 2021-01-19 | |||||||||||
Sponsor Name:IRCCS Fondazione Stella Maris | |||||||||||||
Full Title: Phase 2 pharmacological experimental study to test the safety of miglustat in subjects with hereditary spastic paraplegia type 11 | |||||||||||||
Medical condition: Spastic paraparesis type 11 (SPG11), caused by mutations in spatacsin protein, is characterized by the association of peripheral neuropathy, parkinsonism, ataxia, cognitive impairment, hypotrophy o... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012123-28 | Sponsor Protocol Number: F13640 CP 201 | Start Date*: 2009-07-15 | |||||||||||
Sponsor Name:Institut de Recherche Pierre Fabre | |||||||||||||
Full Title: A dose-finding study of efficacy and safety of F13640 in patients with moderate to severe painful peripheral diabetic polyneuropathy | |||||||||||||
Medical condition: diabetic peripheral neuropathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) DE (Completed) HU (Completed) LT (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003561-17 | Sponsor Protocol Number: 750CNP01 | Start Date*: 2020-01-23 | |||||||||||
Sponsor Name:Toray Industries, Inc. | |||||||||||||
Full Title: A Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TRK-750 in Colorectal Cancer Patients with Chemotherapy-induced Peripheral Neuropathy Following Oxaliplatin-con... | |||||||||||||
Medical condition: Chemotherapy-induced peripheral neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001201-25 | Sponsor Protocol Number: RGH-896-004 | Start Date*: 2005-05-31 |
Sponsor Name:Gedeon Richter Ltd | ||
Full Title: Phase II placebo-controlled study to evaluate the efficacy, safety and tolerability of RGH-896 in patients with pain due to diabetic sensorimotor peripheral neuropathy | ||
Medical condition: Neuropathic pain in patients with diabetic peripheral neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2006-001598-10 | Sponsor Protocol Number: GWDN0603 | Start Date*: 2006-09-26 |
Sponsor Name:GW Pharma Ltd | ||
Full Title: A double blind, randomised, placebo controlled, parallel group study of Sativex® in the treatment of subjects with pain due to diabetic neuropathy | ||
Medical condition: Diabetic Neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006488-22 | Sponsor Protocol Number: E2007-G000-227 | Start Date*: 2007-10-03 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel- Group Trial to Evaluate the Efficacy and Safety of E2007 in Patients with Painful Diabetic Neuropathy | |||||||||||||
Medical condition: Painful Diabetic Neuropathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004188-50 | Sponsor Protocol Number: F1J-MC-HMEM | Start Date*: 2006-02-10 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: Maintenance of Effect of Duloxetine 60 mg Once Daily in Patients with Diabetic Peripheral Neuropathic Pain | ||
Medical condition: Diabetic Peripheral Neuropathic Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002772-27 | Sponsor Protocol Number: 039(B)PO16143 | Start Date*: 2017-03-20 | |||||||||||||||||||||
Sponsor Name:Angelini S.p.A. | |||||||||||||||||||||||
Full Title: Efficacy and safety of low doses of trazodone in patients affected by painful diabetic neuropathy: randomized, controlled, pilot study. | |||||||||||||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) HU (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002523-42 | Sponsor Protocol Number: D5680C00002 | Start Date*: 2018-10-22 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, dose-response study of the efficacy and safety of MEDI7352 in subjects with painful diabetic neuropathy | |||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) PL (Prematurely Ended) HU (Prematurely Ended) DK (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004499-38 | Sponsor Protocol Number: CCR 3116 | Start Date*: 2010-04-16 | |||||||||||
Sponsor Name:Royal Marsden NHS Foundation Trust | |||||||||||||
Full Title: A randomised double-blind placebo-controlled trial of the safety and efficacy of ethosuximide 250mg capsules for the management of chemotherapy-induced painful peripheral neuropathy. | |||||||||||||
Medical condition: The medicial condition under investigation is chemotherapy-induced painful peripheral neuropathy (CIPPN). CIPPN is a complication of several classes of chemotherapy agents e.g taxanes (paclitaxel, ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003968-31 | Sponsor Protocol Number: | Start Date*: 2014-04-09 | |||||||||||
Sponsor Name:University of Edinburgh (ACCORD)
[...]
1. University of Edinburgh (ACCORD)
2. NHS Lothian (ACCORD) |
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Full Title: A phase II RCT of topical menthol gel versus placebo in the treatment of chemotherapy induced peripheral neuropathic pain | |||||||||||||
Medical condition: Chemotherapy Induced Peripheral Neuropathy (CIPN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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