- Trials with a EudraCT protocol (138)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
138 result(s) found for: Polyneuropathy.
Displaying page 1 of 7.
EudraCT Number: 2005-003046-33 | Sponsor Protocol Number: kepp2 | Start Date*: 2005-09-02 |
Sponsor Name:Søren H. Sindrup, Department of Neurology, Odense University Hospital | ||
Full Title: Double-bllind, randomised, placebo-controlled trial of levetiracetam in painful polyneuropathy | ||
Medical condition: Painful polyneuropathy (idiopathic, diabetic, alcoholic, drug-induced and other etiologies) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004007-19 | Sponsor Protocol Number: AV-007-IM | Start Date*: 2006-11-16 | |||||||||||
Sponsor Name:Nycomed Austria GmbH | |||||||||||||
Full Title: A multi-centre, double-blind, placebo-controlled, randomised, parallel group clinical trial to evaluate efficacy and safety of Actovegin® in diabetic type 2 patients with symptomatic diabetic perip... | |||||||||||||
Medical condition: Diabetic Polyneuropathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004794-18 | Sponsor Protocol Number: KF6005/02 | Start Date*: 2009-01-22 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized Phase IIa trial evaluating the safety and efficacy of a new centrally acting analgesic in subjects with pain due to diabetic polyneuropathy | |||||||||||||
Medical condition: painful diabetic polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002843-18 | Sponsor Protocol Number: AS3201-G000-291 | Start Date*: 2009-09-21 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A 2-year, Randomized, Double-blind, Placebo-controlled, Multi-center, Phase II-III Study to Evaluate the Efficacy and Safety of Oral Ranirestat (40 and 80 mg) in Mild to Moderate Diabetic Sensorimo... | |||||||||||||
Medical condition: Diabetic Sensorimotor Polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) EE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003054-16 | Sponsor Protocol Number: DDZ-BOND-2017 | Start Date*: 2018-07-27 | |||||||||||
Sponsor Name:Wörwag Pharma GmbH & co. KG | |||||||||||||
Full Title: Randomized double-blind, placebo-controlled parallel group study over 12 months to assess the effects of treatment with benfotiamine on morphometric, neurophysiological, and clinical measures in ty... | |||||||||||||
Medical condition: diabetic polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002984-40 | Sponsor Protocol Number: beta2 | Start Date*: 2015-09-25 | |||||||||||
Sponsor Name:Department of Neurology, Odense University Hospital | |||||||||||||
Full Title: The beta-2-agonist terbutaline for the treatment of painful polyneuropathy. A randomised, active- and placebo-controlled trial | |||||||||||||
Medical condition: Painful polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001058-85 | Sponsor Protocol Number: WOE_2013_SB | Start Date*: 2013-07-30 | |||||||||||
Sponsor Name:Wörwag Pharma GmbH & Co. KG | |||||||||||||
Full Title: EFFECTS OF BENFOTIAMINE ON INTRAEPIDERMAL NERVE FIBER DENSITY (IENFD) AND DIABETIC NEUROPATHY IN SUBJECTS WITH SENSORIMOTOR DIABETIC POLYNEUROPATHY: A DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, ... | |||||||||||||
Medical condition: Diabetic neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
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: 2020-001285-11 | Sponsor Protocol Number: P20.XXX | Start Date*: 2021-01-12 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A Randomized, open label, Non-inferiority trial on the efficacy of Lacosamide versus Duloxetine in Patients with Chemotherapy-induced Polyneuropathy – A strategy trial | ||
Medical condition: Chemotherapy-induced polyneuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004157-24 | Sponsor Protocol Number: IgPro20_3004 | Start Date*: 2014-04-30 | |||||||||||
Sponsor Name:CSL Behring GmbH | |||||||||||||
Full Title: Multicenter, open-label extension study to investigate the long-term safety and efficacy of IgPro20 in maintenance treatment of chronic inflammatory demyelinating polyneuropathy (CIDP) in subjec... | |||||||||||||
Medical condition: Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) DE (Completed) ES (Completed) FI (Completed) NL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002968-49 | Sponsor Protocol Number: BN43118 | Start Date*: 2022-06-24 | |||||||||||||||||||||
Sponsor Name:Roche Farma S. A. U. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
Full Title: A PHASE III, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY, SAFETY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF CROVALIMAB IN PATIENTS WITH GUILLAIN-BARRÉ S... | |||||||||||||||||||||||
Medical condition: Guillain-Barré syndrome (GBS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003448-28 | Sponsor Protocol Number: IgPro20_3003 | Start Date*: 2012-04-20 | |||||||||||
Sponsor Name:CSL Behring GmbH | |||||||||||||
Full Title: Randomized, multicenter, double-blind, placebo-controlled, parallel-group phase III study to investigate the efficacy, safety, and tolerability of 2 different doses of IgPro20 (subcutaneous immunog... | |||||||||||||
Medical condition: Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) ES (Completed) FI (Completed) NL (Completed) AT (Completed) GB (Completed) IT (Completed) BE (Completed) LT (Prematurely Ended) PL (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004375-12 | Sponsor Protocol Number: TODINELI | Start Date*: 2014-02-13 | |||||||||||||||||||||
Sponsor Name:Center of Mech-Sense | |||||||||||||||||||||||
Full Title: TODINELI Trial A randomized, double-blinded, single-centre, parallel-group, placebo-controlled, prospective trial of the neuroprotective effect of Liraglutide for treatment of diabetic neuropathy | |||||||||||||||||||||||
Medical condition: TODINELI Trial A randomized, double-blinded, single-centre, parallel-group, placebo-controlled, prospective trial of the neuroprotective effect of Liraglutide for treatment of diabetic neuropathy i... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022557-42 | Sponsor Protocol Number: KF6005/04 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized 4-week Phase IIa trial evaluating the efficacy, safety, and tolerability of GRT6005, a new centrally acting analgesic, in subjects with pain due to diabetic polyneuropathy. | |||||||||||||
Medical condition: Pain due to diabetic polyneuropathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005815-17 | Sponsor Protocol Number: OXN2502 | Start Date*: 2009-06-09 | |||||||||||
Sponsor Name:Mundipharma Research GmbH & Co. KG | |||||||||||||
Full Title: An exploratory, randomised, double-blind, single-dummy, placebo controlled, parallel group study to demonstrate the analgesic efficacy of oxycodone/naloxone prolonged release tablets (OXN PR) in ad... | |||||||||||||
Medical condition: Severe pain due to diabetic polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005659-83 | Sponsor Protocol Number: SID2009 | Start Date*: 2010-01-28 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Second IVIg Dose in GBS patients with poor prognosis (SID-GBS trial) | |||||||||||||
Medical condition: Guillian-Barre syndrome | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017672-24 | Sponsor Protocol Number: IgPro10_3001 | Start Date*: 2010-09-13 | |||||||||||
Sponsor Name:CSL Behring GmbH | |||||||||||||
Full Title: A single-arm study to demonstrate the efficacy and safety of Privigen in the treatment of subjects with chronic inflammatory demyelinating polyneuropathy (CIDP) | |||||||||||||
Medical condition: Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000228-33 | Sponsor Protocol Number: GN12NE462 | Start Date*: 2013-11-07 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde [...] | |||||||||||||
Full Title: Inhibition of complement activation (eculizumab®) in Guillain-Barré Syndrome study | |||||||||||||
Medical condition: Guillain-Barré Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013061-26 | Sponsor Protocol Number: DuloTram_1.0 | Start Date*: 2009-07-14 | ||||||||||||||||
Sponsor Name:University of Turku | ||||||||||||||||||
Full Title: Efficacy, safety, tolerability and pharmacokinetics of concomitant administration of tramadol with duloxetine or pregabalin: a randomized controlled flexible-dose study in patients with neuropathic... | ||||||||||||||||||
Medical condition: G53.0 Vyöruusun jälkeinen hermosärky G63.2 Diabeteksen monihermosairaus | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003430-33 | Sponsor Protocol Number: IgPro10_4002 | Start Date*: 2018-09-19 | |||||||||||
Sponsor Name:CSL Behring | |||||||||||||
Full Title: Randomized Study of Single vs. Multiple Privigen Dose Regimens in Pediatric CIDP | |||||||||||||
Medical condition: Pediatric Chronic inflammatory demyelinating polyneuropathy (CIDP) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
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