- Trials with a EudraCT protocol (287)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
287 result(s) found for: Neuropathic pain.
Displaying page 9 of 15.
EudraCT Number: 2012-001586-32 | Sponsor Protocol Number: GN12RE072 | Start Date*: 2012-12-13 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde | |||||||||||||
Full Title: The role of Qutenza (topical capsaicin 8%) in the treatment of chronic pain from critical ischaemia in patients with end stage renal failure | |||||||||||||
Medical condition: Chronic pain from critical limb ischaemia in patients with end-stage renal failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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: 2021-005326-23 | Sponsor Protocol Number: PHRC-K2020PEZET | Start Date*: 2022-01-24 |
Sponsor Name:CHU de Clermont-Ferrand | ||
Full Title: Evaluation of the efficacy of donepezil in the treatment of oxaliplatin-induced peripheral neuropathy: proof of concept study | ||
Medical condition: Oxaliplatine-induced peripheral neuropathy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003300-14 | Sponsor Protocol Number: 74719 | Start Date*: 2020-10-07 |
Sponsor Name:Department of Cardiothoracic Surgery, Aalborg Universityhospital | ||
Full Title: Botulinum Toxin A as Treatment for Chronic Postsurgical Pain Following Lung Cancer Surgery: a Randomized Controlled Pilot Trial | ||
Medical condition: Post Thoracotomy Pain Syndrome (PTPS) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-005470-12 | Sponsor Protocol Number: Calc01 | Start Date*: 2009-05-11 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Calcitonin Prophylaxis in Phantom Limb Pain | |||||||||||||
Medical condition: Almost 60% of patients suffer from phantom limb pain one year after surgery, whereas in the first month, 85% to 97% of patients experience phantom limb pain. IV. calcitonin in the early postoperati... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012094-35 | Sponsor Protocol Number: D5090C00018 | Start Date*: 2009-08-11 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase IIa randomised, double-blind, placebo controlled, parallel group, multicentre study evaluating the efficacy, safety, tolerability and pharmacokinetics of AZD1386 after 3 weeks of treatment... | |||||||||||||
Medical condition: Patients with Posttraumatic Neuralgia (PTN) and Postherpetic Neuralgia (PHN) Intended Indication is Neuropathic Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024265-40 | Sponsor Protocol Number: KETA-FAN | Start Date*: 2011-10-27 | |||||||||||
Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE | |||||||||||||
Full Title: Perineural vs systemic N-methyl-D-aspartate (NMDA) receptors antagonism with ketamine as a reverser of peripheral and central sensitization in phantom limb pain | |||||||||||||
Medical condition: Phantom limb pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002320-25 | Sponsor Protocol Number: UC_0106/1712 | Start Date*: 2018-07-03 |
Sponsor Name:UNICANCER | ||
Full Title: Effectiveness assessment of riluzole in the prevention of oxaliplatin-induced peripheral neuropathy: A phase II randomized study by the UNICANCER with cooperation of AFSOS. | ||
Medical condition: Colorectal cancer stage II/III with adjuvant oxaliplatin-based chemotherapy (simplified FOLFOX4) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020042-94 | Sponsor Protocol Number: LS07-040 | Start Date*: 2010-09-02 |
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin | ||
Full Title: The Effect of High-dose Remifentanil on the Reversal of Neuropathic Pain in Postherpetic Patients | ||
Medical condition: Post herpetic hyperalgesia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002792-41 | Sponsor Protocol Number: Fx-005 | Start Date*: 2006-10-30 | |||||||||||
Sponsor Name:FoldRx Pharmaceuticals Limited | |||||||||||||
Full Title: Safety and Efficacy of Orally Administered Fx-1006A in Patients with Familial Amyloid Polyneuropathy (FAP): a Phase II/III, Randomised, Double-Blind, Placebo-Controlled Study | |||||||||||||
Medical condition: Familial Amyloid Polyneuropathy (FAP). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) PT (Completed) GB (Completed) ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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: 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: 2019-002858-23 | Sponsor Protocol Number: PI2019_843_0051 | Start Date*: 2019-11-20 |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: Serratus plain block versus paravertebral block versus serratus plain block and paravertebral block for postoperative pain following thoracoscopic surgery | ||
Medical condition: postoperative pain following thoracoscopic surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005590-32 | Sponsor Protocol Number: APCP-113 | Start Date*: 2013-02-20 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: A double blind, placebo controlled Phase 2 study comparing the effects of ARA 290 on neuropathic symptoms of patients with type 2 diabetes | ||
Medical condition: Diabetes type 2: neuropathic symptoms | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023461-22 | Sponsor Protocol Number: ET2010-077 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:CENTRE LEON BERARD | |||||||||||||
Full Title: Efficacité et tolérance d’emplâtres de lidocaïne à 5% (Versatis® 5%) dans les douleurs neuropathiques et dans les douleurs de crises vaso-occlusives drépanocytaires de l’enfant, de l’adolescent et ... | |||||||||||||
Medical condition: Enfants, adolescents ou jeunes adultes présentant soit des douleurs neuropathiques pures ou mixtes soit des douleurs de crises vaso-occlusives drépanocytaires, localisées, superficielles | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001703-37 | Sponsor Protocol Number: D-FR-52120-244 | Start Date*: 2018-09-06 | |||||||||||
Sponsor Name:Ipsen Innovation SAS | |||||||||||||
Full Title: A double-blind, randomised, placebo controlled, proof-of-concept study in subjects with abdominal or thoracic chronic scar pain to assess the analgesic properties of intradermal doses of Dysport® | |||||||||||||
Medical condition: Post-Surgical neuralgia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004196-37 | Sponsor Protocol Number: PA02-124 1 RO1AT002146-01 | Start Date*: 2006-09-22 |
Sponsor Name:University of Birmingham, Research & Enterprise Services [...] | ||
Full Title: Taurine and Painful Diabetic Neuropathy | ||
Medical condition: Diabetic painful peripheral neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-000234-57 | Sponsor Protocol Number: allo-APZ2-DFU-II-01 | Start Date*: 2017-08-07 | |||||||||||
Sponsor Name:RHEACELL GmbH & Co. KG | |||||||||||||
Full Title: An interventional, multicenter, single arm, phase I/IIa clinical trial to investigate the efficacy and safety of allo-APZ2-DFU on wound healing of diabetic neuropathic ulcer (DFU). | |||||||||||||
Medical condition: Diabetic neuropathic ulcer (DFU) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000133-12 | Sponsor Protocol Number: 039(1)PO16357 | Start Date*: 2018-10-26 | |||||||||||||||||||||
Sponsor Name:Angelini S.p.A. | |||||||||||||||||||||||
Full Title: Efficacy and safety of Fixed-Dose Combination (FDC) products containing trazodone and gabapentin in patients affected by painful diabetic neuropathy: randomized, controlled, dose finding study. | |||||||||||||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) GB (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006184-70 | Sponsor Protocol Number: PM07/8404 | Start Date*: 2009-01-09 |
Sponsor Name:The Leeds Teaching Hospitals NHS Trust | ||
Full Title: A POPULATION STUDY INTO THE PREVALENCE AND GENETIC PROFILE OF PATIENTS WITH CHRONIC PAIN WHO DO NOT RESPOND TO ORAL CODEINE A single site, pilot population study into the prevalence and genetic p... | ||
Medical condition: Chronic pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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