- Trials with a EudraCT protocol (313)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
313 result(s) found for: Peripheral nervous system.
Displaying page 1 of 16.
EudraCT Number: 2006-000526-31 | Sponsor Protocol Number: BT2006003 | Start Date*: 2007-01-03 | |||||||||||
Sponsor Name:Section of Clinical Pain Research, Department of Molecular Medicine and Surgery Karolinska Institute | |||||||||||||
Full Title: Brush-evoked allodynia in patients with peripheral neuropathy before and following intravenous infusion of ondansetron. A randomised, double-blind, placebo controlled, cross-over study. | |||||||||||||
Medical condition: Peripheral neuropathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000585-30 | Sponsor Protocol Number: I16016 | Start Date*: 2017-12-13 | ||||||||||||||||
Sponsor Name:CHU de Limoges | ||||||||||||||||||
Full Title: Pilot study, single-blind, candesartan versus usual care of peripheral neuropathy development induced by vincristine (PNIV) in patients treated for lymphoma B. | ||||||||||||||||||
Medical condition: peripheral neuropathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-013643-11 | Sponsor Protocol Number: DN01 | Start Date*: 2009-08-30 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
Full Title: Neuroprotective effects of palmitoylethanolamide in diabetic neuropathy: a pilot study. | |||||||||||||
Medical condition: diabetic neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000012-24 | Sponsor Protocol Number: DOXATTR | Start Date*: 2006-01-24 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: A phase II study of the safety and efficacy of doxycycline administered cyclically in patients suffering from Transthyretin Amiloidosis ATTR | |||||||||||||
Medical condition: Transthyretin amyloidosis ATTR | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001204-36 | Sponsor Protocol Number: BUP20050001 | Start Date*: 2005-08-01 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||
Full Title: Open pilot study for the evaluation of the analgesic effect of buprenorphine TDS administered as add-on treatment in patients with chronic neuropathic pain inadequately controlled by conventional t... | |||||||||||||
Medical condition: Chronic neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000032-27 | Sponsor Protocol Number: GUP05007 | Start Date*: 2005-10-19 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||
Full Title: MULTICENTRE RANDOMISED DOUBLE BLIND PLACEBO CONTROLLED TRIAL OF LONG-TERM ASCORBIC ACID TREATMENT IN CHARCOT-MARIE-TOOTH DISEASE TYPE 1A CMT-TRIAAL CMT-TRial Italian with Ascorbic Acid Long term | |||||||||||||
Medical condition: Charcot-Marie-Tooth disease type 1A CMT1A | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002609-24 | Sponsor Protocol Number: LESVIPREGA/20/P3-3 | Start Date*: 2021-05-17 | |||||||||||
Sponsor Name:Laboratorios Lesvi, S.L. (Neuraxpharm group) | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled, Multicenter, Phase 3 Clinical Study to Evaluate Efficacy and Safety of the Once-Daily Extended-Release Pregabalin and the Immediate-Release Pregabali... | |||||||||||||
Medical condition: Peripheral neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PL (Completed) HU (Completed) BG (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002917-11 | Sponsor Protocol Number: A0081124 | Start Date*: 2006-11-02 | |||||||||||
Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF THE PREVENTION AND TREATMENT OF CHEMOTHERAPY-INDUCED PERIPHERAL NEUROPATHY SYMPTOMS WITH PREGABALIN IN SUBJECTS WITH ADVANCED COLORECTAL CANCER | |||||||||||||
Medical condition: CHEMOTHERAPY-INDUCED PERIPHERAL NEUROPATHY SYMPTOMS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002131-32 | Sponsor Protocol Number: SP001033 | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA PER LO STUDIO DEL DOLORE | |||||||||||||
Full Title: A RANDOMIZED, OPEN COMPARISON BETWEEN PREGABALIN/TRANSDERMAL BUPRENORPHINE AND PREGABALIN/DICLOFENAC IN CHRONIC NEUROPATHIC PAIN PATIENTS | |||||||||||||
Medical condition: PERIPHERAL NEUROPATHIC PAIN DUE TO POST-HERPETIC NEURALGIA OR DIABETIC POLYNEUROPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002258-30 | Sponsor Protocol Number: M/SATIVX/01 | Start Date*: 2011-10-04 | |||||||||||
Sponsor Name:ALMIRALL PRODESFARMA | |||||||||||||
Full Title: NEUROPHYSIOLOGIC STUDY AIMED AT EVALUATING ON EFFECT OF SATIVEX® ON SPASTICITY IN PROGRESSIVE MULTIPLE SCLEROSIS | |||||||||||||
Medical condition: Subject of both male and female gender affected by Secondary-Progressive (SP) or Primary-Progressive (PP) MS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003110-40 | Sponsor Protocol Number: LACOSAMIDE-2018 | Start Date*: 2018-09-11 | |||||||||||
Sponsor Name:Aarhus University | |||||||||||||
Full Title: The effect of lacosamide in peripheral neuropathic pain: a randomized, double-blind, placebo-controlled, phenotype-stratified study | |||||||||||||
Medical condition: Peripheral Neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004410-42 | Sponsor Protocol Number: C11-09 | Start Date*: 2012-11-26 | |||||||||||||||||||||
Sponsor Name:Inserm | |||||||||||||||||||||||
Full Title: A phase I/II, open labeled, monocentric study of direct intracranial administration of a replication deficient adeno-associated virus gene transfer vector serotype rh.10 expressing the human ARSA c... | |||||||||||||||||||||||
Medical condition: Early onset forms of MLD | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000243-27 | Sponsor Protocol Number: BUPROPION2019 | Start Date*: 2019-03-18 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: The effect of bupropion in peripheral neuropathic pain. A randomized, double-blind, placebo-controlled study. | |||||||||||||
Medical condition: Peripheral neuropathic , i.e. painful polyneuropathy, postherpetic neuralgia and pain after nerve injury (traumatic or surgical). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005127-40 | Sponsor Protocol Number: M13-383 | Start Date*: 2012-03-01 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo- and Active Controlled Study of the Electrophysiological Effects of ABT-639 on Spontaneous Activity in C Nociceptors in Patients with Diabetic Peripheral Neuropa... | |||||||||||||
Medical condition: Diabetec Neuropathic Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002225-19 | Sponsor Protocol Number: FE001 | Start Date*: 2016-01-18 |
Sponsor Name:Diagnostic Centre of Pécs | ||
Full Title: Ferumoxytol as an MR contrast agent in CNS and head & neck tumors, intracranial and peripheral vascular disease | ||
Medical condition: Feraheme will be tested as an MRI contrast agent in the diseases of the central nervous system, in head and neck tumors and peripheral vascular diseases. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005198-38 | Sponsor Protocol Number: CANNA1 | Start Date*: 2018-10-26 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Tetra-hydro-cannabinol, cannabidiol and their combination for the treatment of peripheral neuropathic pain. A randomised placebo-controlled trial. | |||||||||||||
Medical condition: Peripheral neuropathic pain due to polyneuropathy, postherpetic neuralgia, or peripheral nerve injury (surgical or traumatic). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003382-16 | Sponsor Protocol Number: RMC1 | Start Date*: 2005-11-10 |
Sponsor Name:Guy's & St Thomas's NHS Foundation Trust [...] | ||
Full Title: Pilot randomised controlled trial of methotrexate for chronic inflammatory demyelinating polyradiculoneuropathy (RMC trial). | ||
Medical condition: Chronic inflammatory demyelinating polyradiculoneuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000398-21 | Sponsor Protocol Number: ESTEVE-SIGM-202 | Start Date*: 2012-06-21 | |||||||||||
Sponsor Name:Laboratorios del Dr. Esteve, S.A. | |||||||||||||
Full Title: A proof-of-concept phase 2, randomized, placebo-controlled, double blind, multicentre clinical trial in 2 parallel groups to evaluate the efficacy and safety of E-52862 for reducing the incidence a... | |||||||||||||
Medical condition: OXL-induced chronic neuropathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000559-26 | Sponsor Protocol Number: PRAG-MS | Start Date*: 2017-09-14 | |||||||||||||||||||||
Sponsor Name:FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||||||||||||
Full Title: A multicentric randomized PRAGmatic trial to compare the effectiveness of fingolimod versus dimethyl-fumarate on patient overall disease experience in relapsing remitting Multiple Sclerosis: novel... | |||||||||||||||||||||||
Medical condition: relapsing-remitting multiple sclerosis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006319-69 | Sponsor Protocol Number: 1.0 | Start Date*: 2012-10-25 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Pedro Villarejo Campos(Hospital Universitario Ciudad Real) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Closed abdomen hyperthermic intraperitoneal chemotherapy with paclitaxel for advanced epithelial ovarian cancer | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: ovarian cancer (II,III,IV FIGO staging and tumoral recurrence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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