- Trials with a EudraCT protocol (19)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
19 result(s) found for: Radiculopathy.
Displaying page 1 of 1.
| EudraCT Number: 2010-023962-39 | Sponsor Protocol Number: 1014802/201 | Start Date*: 2011-03-09 | ||||||||||||||||
| Sponsor Name:Convergence Pharmaceuticals Ltd | ||||||||||||||||||
| Full Title: A randomized, double blind, cross-over study to evaluate the safety and efficacy of CNV1014802 in subjects with neuropathic pain from lumbosacral radiculopathy | ||||||||||||||||||
| Medical condition: Neuropathic pain from lumbosacral radiculopathy | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Completed) CZ (Completed) DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-004775-78 | Sponsor Protocol Number: 1014802-203 | Start Date*: 2016-05-09 | ||||||||||||||||
| Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of BIIB074 in Subjects With Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
| Medical condition: Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: LV (Completed) GB (Completed) CZ (Completed) SK (Completed) AT (Completed) ES (Completed) NL (Completed) BE (Completed) FR (Completed) RO (Completed) BG (Completed) LT (Prematurely Ended) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-012836-33 | Sponsor Protocol Number: KIP113049 | Start Date*: 2009-11-26 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
| Full Title: A randomised, double blind study to evaluate the safety and efficacy of the p38 kinase inhibitor, GW856553, in subjects with neuropathic pain from lumbosacral radiculopathy | |||||||||||||
| Medical condition: Neuropathic pain from lumbosacral radiculopathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DE (Completed) DK (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004796-68 | Sponsor Protocol Number: 1014802-204 | Start Date*: 2016-10-26 | ||||||||||||||||
| Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
| Full Title: An Uncontrolled, Open-Label Extension Study to Evaluate the Long Term Safety, Tolerability, and Maintenance of Effect of BIIB074 in Subjects With Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
| Medical condition: Neuropathic Pain From Lumbosacral Radiculopathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: LV (Completed) GB (Completed) SK (Completed) AT (Completed) ES (Completed) CZ (Completed) BG (Completed) BE (Completed) NL (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-002632-90 | Sponsor Protocol Number: OF_NEIR_CT1 | Start Date*: 2020-11-09 |
| Sponsor Name:"Olainfarm" AS | ||
| Full Title: A prospective, double-blind, randomised, placebo-controlled trial on the efficacy and safety of Neiromidin 20 mg tablets in the treatment of patients with lumbosacral radiculopathy | ||
| Medical condition: Lumbosacral radiculopathy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: PL (Completed) CZ (Completed) LV (Completed) BG (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-006503-15 | Sponsor Protocol Number: STA-LDH01 | Start Date*: 2023-02-23 | |||||||||||||||||||||
| Sponsor Name:Stayble Therapeutics | |||||||||||||||||||||||
| Full Title: A prospective, randomised, double-blinded, placebo-controlled study investigating the safety and tolerability of STA363 in patients with radiculopathy caused by lumbar disc herniation | |||||||||||||||||||||||
| Medical condition: Radiculopathy due to lumbar intervertebral disc herniation | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2004-002948-10 | Sponsor Protocol Number: A0081007 | Start Date*: 2005-07-14 | |||||||||||
| Sponsor Name:Pfizer AB | |||||||||||||
| Full Title: A Randomised Placebo-Controlled Trial of the Efficacy and Safety of Pregabalin in the Treatment of Subjects with Neuropathic Pain Associated with Lumbo-sacral Radiculopathy (protocol dates 2004-11... | |||||||||||||
| Medical condition: Pain associated with lumbo-sacral radiculopathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DE (Completed) IT (Completed) ES (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: 2012-003160-44 | Sponsor Protocol Number: 191177 | Start Date*: 2013-04-30 | |||||||||||
| Sponsor Name:Orthopaedic Research Laboratory, Århus University Hospital | |||||||||||||
| Full Title: Treatment of moderate intervertebral disc degeneration with autologous bonemarrow derived mesenchymal stem cells (bMSC): | |||||||||||||
| Medical condition: Moderate intervertebral disc degeneration without radiculopathy | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-006176-30 | Sponsor Protocol Number: NW-1029/01-08 | Start Date*: 2009-03-13 | |||||||||||
| Sponsor Name:Newron Pharmaceuticals S.p.A. | |||||||||||||
| Full Title: EFFICACY AND SAFETY OF TWO FIXED DOSES (160 OR 320 MG/DAY) OF RALFINAMIDE IN PATIENTS WITH CHRONIC NEUROPATHIC LOW BACK PAIN. A MULTICENTER, DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED 12- WEEK ST... | |||||||||||||
| Medical condition: Chronic neuropathic low back pain. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Prematurely Ended) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2020-002849-42 | Sponsor Protocol Number: RC-P0103 | Start Date*: 2021-04-21 | |||||||||||||||||||||
| Sponsor Name:GROUPEMENT DES HOPITAUX DE L'INSTITUT CATHOLIQUE DE LILLE | |||||||||||||||||||||||
| Full Title: | |||||||||||||||||||||||
| Medical condition: | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2006-001072-21 | Sponsor Protocol Number: MKN106762 | Start Date*: 2006-08-08 |
| Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||
| Full Title: A double-blind placebo-controlled study of the efficacy and safety of the P38 Map Kinase inhibitor SB681323 in patients with neuropathic pain following nerve trauma | ||
| Medical condition: Neuropathic pain | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-006235-33 | Sponsor Protocol Number: 738/02/2011 | Start Date*: 2012-03-30 | |||||||||||
| Sponsor Name:MDM S.P.A. | |||||||||||||
| Full Title: Sensory Motor Neuropathies of the sciatic nerve: a comparative evaluation of dextrorotatory enantiomer of thioctic acid and acetyl-L-carnitine. | |||||||||||||
| Medical condition: sensitive motor sciatic neuropathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000675-34 | Sponsor Protocol Number: EU 101 | Start Date*: 2004-12-21 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: A Prospective, Randomized, Controlled, Multi-center, (Pilot) Study of Osigraft® in Instrumented Posterolateral Fusions | ||
| Medical condition: Subjects qualifying for decompression and fusion of one spinal level (L3-S1) with the use of autograft will be recruited through the medical institutions of participating investigators. All subject... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002751-25 | Sponsor Protocol Number: RG112-14 | Start Date*: 2014-10-08 | |||||||||||
| Sponsor Name:The Walton Centre NHS Foundation Trust | |||||||||||||
| Full Title: Multi-centre randomised control trial comparing the clinical and cost effectiveness of trans-foraminal epidural steroid injection to surgical microdiscectomy for the treatment of chronic radicular ... | |||||||||||||
| Medical condition: Chronic radicular pain secondary to a prolapsed intervertebral disc herniation | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001195-21 | Sponsor Protocol Number: SFK3 | Start Date*: 2015-10-19 |
| Sponsor Name:Sørlandet Hospital | ||
| Full Title: NoTOPain Novel Treatment Option for neuropathic Pain A randomized, cross-over, placebo-controlled, double-blind, single-center, phase II study of cetuximab in patients with treatment-refracto... | ||
| Medical condition: Neuropathic pain conditions, i.e. radiculopathy or Complex regional pain syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003656-37 | Sponsor Protocol Number: MEIN/18/DEX-LBP/001 | Start Date*: 2020-06-04 | |||||||||||
| Sponsor Name:Menarini International Operations Luxembourg SA | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, parallel arm group study to evaluate the analgesic efficacy and safety of dexketoprofen trometamol and tramadol hydrochloride oral fixed dose combina... | |||||||||||||
| Medical condition: Low back pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: EE (Completed) PL (Completed) ES (Completed) HU (Completed) LV (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007478-39 | Sponsor Protocol Number: 42160443NPP2001 | Start Date*: 2009-10-07 | |||||||||||||||||||||
| Sponsor Name:Janssen Cilag International, NV | |||||||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 in Subjects With Postherpetic Neuralgia and Post-T... | |||||||||||||||||||||||
| Medical condition: Postherpetic Neuralgia and Post-Traumatic Neuralgia | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) NL (Prematurely Ended) ES (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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