- Trials with a EudraCT protocol (221)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
221 result(s) found for: Peripheral nerve.
Displaying page 1 of 12.
EudraCT Number: 2009-016038-29 | Sponsor Protocol Number: LIDO-2009 | Start Date*: 2010-03-11 | ||||||||||||||||
Sponsor Name:Danish Pain Research Center | ||||||||||||||||||
Full Title: Topical lidocaine: Predictors of response in peripheral nerve damage | ||||||||||||||||||
Medical condition: Neuropathic pain due to Peripheral nerve damage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-018143-25 | Sponsor Protocol Number: 2010 | Start Date*: 2010-05-06 | ||||||||||||||||
Sponsor Name:Västra Götalandsregionen | ||||||||||||||||||
Full Title: An open label, historical control, study to assess the impact on bacteriological healing of Prednisolone in patients with neuroborreliosis-caused peripheral facial palsy receiving treatment with Do... | ||||||||||||||||||
Medical condition: Facialispares orsakad av CNS-infektion med Borrelia burgdorferi. (Neuroborrelios-orsakad facialispares) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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: 2006-000526-31 | 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: 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: 2005-003409-98 | Sponsor Protocol Number: HERA-05/001 | Start Date*: 2006-02-09 |
Sponsor Name:Hôpital Erasme, Cliniques Universitaires de Bruxelles | ||
Full Title: Enhancement by tacrolimus of nerve regeneration after peripheral nerve repair. | ||
Medical condition: Patients presenting a total section of a major nerve at the arm, forearm, or leg, and treated by conventional nerve suture under microscope within ten days of the trauma. Patients with nerve autogr... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002083-25 | Sponsor Protocol Number: LIDO2011 | Start Date*: 2011-12-05 | ||||||||||||||||
Sponsor Name:BG University Hospital Bergmannsheil GmbH | ||||||||||||||||||
Full Title: Is there a correlation between the pain relief and the A-delta- and C-fiber function after topical application of lidocaine (5%) in patients with peripheral neuropathic pain? | ||||||||||||||||||
Medical condition: Patients with proven diagnosis of painful peripheral neuropathic pain syndromes as diagnosed as: 1. Peripheral nerve lesion or 2. Postherpetic neuralgia. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002303-14 | Sponsor Protocol Number: A5951110 | Start Date*: 2008-12-17 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY10017, USA | |||||||||||||
Full Title: PROSPECTIVE STUDY OF OPHTHALMOLOGIC FUNCTION IN PATIENTS RECEIVING LINEZOLID FOR TWO MONTHS OR GREATER | |||||||||||||
Medical condition: This study is designed to understand the effects of linezolid on the optic nerve by observing and following patients who have been treated with linezolid for two months or longer for the developmen... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005605-27 | Sponsor Protocol Number: TNG908-C101 | Start Date*: 2022-09-07 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Tango Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Phase 1: • Locally advanced or metastatic MTAP-deleted solid tumors (with the exception of gliomas) Phase 2: • Arm 1: Locally advanced or metastatic MTAP-deleted squamous and nonsquamous NSCLC ... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003201-30 | Sponsor Protocol Number: 1.0-03.10.2022 | Start Date*: 2022-12-22 |
Sponsor Name:Medical University Vienna | ||
Full Title: The Impact of Biological Gender in Peripheral Nerve Blockade: A Prospective Study in Volunteers | ||
Medical condition: To evaluate pharmacodynamic, pharmacokinetic and nerve-related morphometric differences of biological gender (male versus female) on nerve block characteristics | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
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: 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: 2014-005656-26 | Sponsor Protocol Number: 51748.094.15 | Start Date*: 2015-10-14 | ||||||||||||||||
Sponsor Name:Westfriesgasthuis | ||||||||||||||||||
Full Title: Amitriptyline 10% and ketamine 10% cream in neuropathic pain: A randomised, double-blind, placebo-controlled cross-over pilot study with a three months open follow-up | ||||||||||||||||||
Medical condition: Patients with peripheral neuropathic pain or scar pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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: 2017-004187-35 | Sponsor Protocol Number: FACE-01 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Falun Hospital | |||||||||||||
Full Title: The FACE (Facial nerve palsy And Cortisone Evaluation) study in children: a randomised double-blind, placebo-controlled, multicenter trial. | |||||||||||||
Medical condition: Facial Nerve Palsy (Bells Palsy) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000348-14 | Sponsor Protocol Number: NSTATIN | Start Date*: 2014-03-05 |
Sponsor Name:Odense University Hospital, Department of Neurology | ||
Full Title: Statin-treatment and peripheral neuropathy - a randomized clinical trial | ||
Medical condition: Patients with cerebral infarction or transient ischemic attack. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-002280-18 | Sponsor Protocol Number: FIPRA#3 | Start Date*: 2017-09-18 | |||||||||||
Sponsor Name:Nordsjællands Hospital Hillerød | |||||||||||||
Full Title: Catheter-based peripheral regional anaesthesia after orthopaedic surgery: Comparison of low dose, automated periodic infusions with conventional high dose, continuous infusion, and patient-initiat... | |||||||||||||
Medical condition: Postoperative pain, after orthopaedic surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001246-17 | Sponsor Protocol Number: CBX129801-DN-201 | Start Date*: 2013-05-28 |
Sponsor Name:Cebix Incorporated | ||
Full Title: A Phase 2b, Randomized, Double-Blind, Placebo Controlled Study to Evaluate the Safety and Efficacy of CBX129801 (Ersatta™), Long-Acting Synthetic C-Peptide, in Type 1 Diabetes Mellitus Subjects wit... | ||
Medical condition: Mild to moderate diabetic peripheral neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
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