- 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 4 of 15.
EudraCT Number: 2016-001353-41 | Sponsor Protocol Number: NL56714.029.16 | Start Date*: 2016-06-06 |
Sponsor Name:VU University medical center Amsterdam | ||
Full Title: Oxygenation of Affected Limbs in CRPS-I Patients | ||
Medical condition: Complex Regional Pain Syndrome, Neuropathic Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003933-32 | Sponsor Protocol Number: A092358 | Start Date*: 2011-09-21 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
Full Title: A randomised, blind, placebo controlled crossover study of the influence of the HCN channel-blocker ivabradine on the symptoms of neuropathic pain | |||||||||||||
Medical condition: Neuropathic Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003502-28 | Sponsor Protocol Number: AP-325.04 | Start Date*: 2020-02-14 | |||||||||||
Sponsor Name:Algiax Pharmaceuticals GmbH | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of AP-325 in Subjects with Peripheral Post-surgical Neuropathic Pain | |||||||||||||
Medical condition: Peripheral post-surgical neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002824-16 | Sponsor Protocol Number: 03-624 | Start Date*: 2004-12-21 |
Sponsor Name:Karolinska Universitetssjukhuset | ||
Full Title: Spinalt klonidin och baklofen som adjuvans till ryggmärgsstimulering vid terapiresistent smärta. (Möjlighet att förstärka den smärtlindrande effekten av alektrisk tyggmärgsstimulering med läkemedel... | ||
Medical condition: Neuropathic pain patients with insufficient pain-relief of trial spinal cord stimulation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003617-17 | Sponsor Protocol Number: NCT03348735 | Start Date*: 2018-12-03 |
Sponsor Name:Antwerp University Hospital (UZA) | ||
Full Title: Efficacy, patient acceptability and safety of topical treatment versus systemic treatment: a randomized, multicenter, comparative pragmatic trial in adult patients suffering from diverse localized ... | ||
Medical condition: Patients suffering from localized neuropathic pain (LNP) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005506-32 | Sponsor Protocol Number: Dulo2006 | Start Date*: 2007-03-05 | |||||||||||
Sponsor Name:Danish Pain Research Center | |||||||||||||
Full Title: Pain, anxiety and depression in neuropathic and non-neuropathic pain: Effect of monoamine modulation. | |||||||||||||
Medical condition: Chronic pain: neuropathic pain and fibromyalgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002560-34 | Sponsor Protocol Number: F1J-US-HMFR(b) | Start Date*: 2008-09-02 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Trial of the Efficacy and Safety of Duloxetine HCl in Patients with Central Neuropathic Pain Due to Multiple Sclerosis | |||||||||||||
Medical condition: Central neuropathic pain due to Multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002080-27 | Sponsor Protocol Number: KPS 2008-01 | Start Date*: 2008-08-06 | ||||||||||||||||
Sponsor Name:Greater Glasgow Health Board/University of Glasgow | ||||||||||||||||||
Full Title: A randomised, double-blind controlled trial of ketamine versus placebo in conjunction with best pain management in neuropathic pain in cancer patients | ||||||||||||||||||
Medical condition: Patients who have neuropathic pain related to cancer and/or treatment for cancer (surgical, chemotherapy or radiotherapy) which has resulted in neuropathic pain. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000347-28 | Sponsor Protocol Number: KF10004/10 | Start Date*: 2012-09-03 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: Efficacy and safety of lidocaine 5% medicated plaster in localized chronic post-operative neuropathic pain | |||||||||||||
Medical condition: moderate to severe localized chronic post-operative neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) ES (Completed) IT (Completed) DK (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001409-64 | Sponsor Protocol Number: AV001 | Start Date*: 2021-09-16 | |||||||||||
Sponsor Name:Averitas Pharma, Inc. | |||||||||||||
Full Title: An interventional, Phase III, double-blind, randomized, controlled, parallel-group, multi-site, clinical trial evaluating the efficacy and safety of Qutenza® in subjects with post-surgical neuropat... | |||||||||||||
Medical condition: Post-surgical neuropathic pain (PSNP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Trial now transitioned) NL (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001140-47 | Sponsor Protocol Number: M10-014 | Start Date*: 2007-12-07 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Global, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Comparing the Safety and Efficacy of ABT-894 versus Placebo in Subjects with Diabetic Neuropathic Pain | |||||||||||||
Medical condition: diabetic neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) DE (Completed) CZ (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001420-35 | Sponsor Protocol Number: LBP_Caps_v1 | Start Date*: 2012-06-05 |
Sponsor Name:Abteilung für Anästhesie, Intensiv- und Schmerzmedizin, Wilhelminenspital der Stadt Wien | ||
Full Title: The effect of a single skin treatment with Capsaicine 8% in low back pain | ||
Medical condition: chronic low back pain with neuropathic pain component or unclear neuropathic pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004897-40 | Sponsor Protocol Number: GABA-2 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:PHARM – Pharmaceutical Research Management srl | |||||||||||||
Full Title: Randomized, double-blind, placebo controlled, multi-centre, superiority phase II study to evaluate the safety, pharmacokinetic, efficacy of gabapentin liquid formulation as add-on to morphine in ch... | |||||||||||||
Medical condition: Chronic pain of neuropathic or mixed origin | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Ongoing) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003048-78 | Sponsor Protocol Number: A0081064 | Start Date*: 2006-02-01 | |||||||||||
Sponsor Name:Pfizer AB | |||||||||||||
Full Title: Full title of the trial: A 9 Week, Randomized, Double-Blind, placebo-controlled, Multicenter, Study of Pregabalin (BID) in subjects with posttraumatic peripheral neuropathic pain | |||||||||||||
Medical condition: Posttraumatic peripheral neuropathic pain in adults | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DK (Completed) FI (Completed) IT (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004395-36 | Sponsor Protocol Number: GWCL0404 | Start Date*: 2005-07-01 |
Sponsor Name:GW Pharma Ltd | ||
Full Title: A Multicentre, Open Label, Follow on Study to Assess the Maintenance of Effect, Tolerance and Safety of Sativex in the Treatment of Subjects with Neuropathic Pain. This will be followed by a random... | ||
Medical condition: Neuropathic pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) CZ (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003638-40 | Sponsor Protocol Number: XTL B07-001 | Start Date*: 2008-01-08 | |||||||||||
Sponsor Name:XTL Development Inc. | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo-controlled, Parallel, Multicenter Study of the Safety and Efficacy of Two Dosages of Bicifadine SR in Adult Outpatients with Chronic Neuropathic Pain Associated ... | |||||||||||||
Medical condition: Chronic neuropathic pain in patients with diabetic peripheral neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005872-41 | Sponsor Protocol Number: QTZ-EC-0004 | Start Date*: 2012-04-25 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||
Full Title: QUTENZA versus pregabalin in subjects with peripheral neuropathic pain: an open-label, randomized, multicenter, noninferiority efficacy and tolerability study | |||||||||||||
Medical condition: Patients who have a documented diagnosis of probable or definite Peripheral Neuropathic Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) FI (Completed) AT (Completed) SK (Completed) ES (Completed) BE (Completed) SI (Completed) GB (Completed) DE (Completed) GR (Completed) PT (Completed) IT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004851-30 | Sponsor Protocol Number: GABA-1 | Start Date*: 2016-08-01 | |||||||||||
Sponsor Name:PHARM – Pharmaceutical Research Management srl | |||||||||||||
Full Title: Randomized, double-blind, double-dummy, active controlled, multicentre, non-inferiority phase-III study to compare the pharmacokinetic, efficacy and safety of gabapentin liquid formulation to trama... | |||||||||||||
Medical condition: Chronic pain of neuropathic or mixed origin | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Completed) FR (Ongoing) GR (Prematurely Ended) GB (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002315-98 | Sponsor Protocol Number: MedicalcannabisMSSCI2018 | Start Date*: 2018-12-06 | ||||||||||||||||
Sponsor Name:Aarhus Universitetshospital | ||||||||||||||||||
Full Title: The effect of medical cannabis on neuropathic pain and spasticity in patients with Multiple Sclerosis and in patients with spinal cord injury. A multicenter national placebo-controlled trial | ||||||||||||||||||
Medical condition: Central neuropathic pain and spasticity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001022-57 | Sponsor Protocol Number: Qutenza-FM-20 | Start Date*: 2020-12-18 | ||||||||||||||||
Sponsor Name:Wojciech Zbigniew Pawlak | ||||||||||||||||||
Full Title: The effect of Qutenza application in patients with post-operative neuropathic pain: A double-blind, randomized, controlled pilot study | ||||||||||||||||||
Medical condition: Post-operative neuropathic pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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