- Trials with a EudraCT protocol (72)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
72 result(s) found for: Lumbar region.
Displaying page 1 of 4.
EudraCT Number: 2016-002887-14 | Sponsor Protocol Number: 2.0 | Start Date*: 2016-10-31 | |||||||||||
Sponsor Name:University of Turku | |||||||||||||
Full Title: Dose response study of Patient Controlled Analgesia (PCA) of S-ketamine in orthopaedic spine surgery patients | |||||||||||||
Medical condition: Patients who are scheduled for elective posterolateral lumbar spine fusion with bilateral transpedicular screw instrumentation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003252-31 | Sponsor Protocol Number: 2.0 | Start Date*: 2015-05-15 | |||||||||||
Sponsor Name:University of Turku | |||||||||||||
Full Title: Dose response study of Patient Controlled Analgesia (PCA) of Dexmedetomidine in orthopaedic spine surgery patients | |||||||||||||
Medical condition: Patients, who are scheduled for elective posterolateral lumbar spine fusion with bilateral transpedicular screw instrumentation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006152-36 | Sponsor Protocol Number: 1774 | Start Date*: 2012-05-10 | |||||||||||
Sponsor Name:Middelfart Rygsektor | |||||||||||||
Full Title: Postoperative treatment with parathyroidea hormone Forteo® in patients undergoing posterolateral spinal fusion surgery. A prospektive and a randomized double-blinded, placebo-controlled study | |||||||||||||
Medical condition: Spinal stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000747-26 | Sponsor Protocol Number: KETTO201200047426 | Start Date*: 2012-04-27 | |||||||||||
Sponsor Name:Helsinki Universiy Central Hospital | |||||||||||||
Full Title: Administration of S-Ketamine during spinal surgery to reduce postoperative pain | |||||||||||||
Medical condition: adult patients undergoing spinal surgery | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000751-25 | Sponsor Protocol Number: AXS02II201501 | Start Date*: 2016-05-02 | |||||||||||
Sponsor Name:Jaro Karppinen | |||||||||||||
Full Title: ZOLEDRONIC ACID, A LONG-ACTING BISPHOSPHONATE, FOR CHRONIC LOW BACK PAIN DUE TO MODIC CHANGES: A RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Chronic low back pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2021-006042-13 | Sponsor Protocol Number: MEDI-TOLP-01 | Start Date*: 2022-03-28 | |||||||||||
Sponsor Name:MEDITOP Gyógyszeripari Kft. | |||||||||||||
Full Title: A randomized double blind placebo controlled multicenter study to assess the efficacy and tolerability of tolperisone as add on treatment with standardized NSAID of acute non specific low back pain. | |||||||||||||
Medical condition: Acute, non-specific low back pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005722-35 | Sponsor Protocol Number: H--6-2014-070 | Start Date*: 2015-06-23 | ||||||||||||||||
Sponsor Name:Glostrup University Hospital | ||||||||||||||||||
Full Title: Measures of inflammation in low back pain (LBP) and anti-TNFα for the treatment of deemed discogenic LBP - an explorative study | ||||||||||||||||||
Medical condition: Low back pain with and without legg-pain In the late periode 1990ies it became clear that various cytokines and other inflammatory elements played a large role for low back pain. One of the known ... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001742-29 | Sponsor Protocol Number: XIL02/15 | Start Date*: 2015-08-25 | |||||||||||
Sponsor Name:INDENA S.P.A. | |||||||||||||
Full Title: Tolerability, safety and activity of IDN5243, 4 mg bid intramuscularly in the treatment of low back pain. A prospective, open label, single-center, uncontrolled study. | |||||||||||||
Medical condition: Low Back Pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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: 2015-002476-24 | Sponsor Protocol Number: EP-DICLO-TIO/F-01-2015 | Start Date*: 2015-10-13 | |||||||||||
Sponsor Name:Epifarma S.r.l. | |||||||||||||
Full Title: Randomized, double-blind, parallel-groups, active-controlled trial to evaluate the efficacy of a fixed combination of diclofenac 75 mg + thiocolchicoside 4 mg as solution for injection, in improvin... | |||||||||||||
Medical condition: low back pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002875-20 | Sponsor Protocol Number: KCT03/2015–DORETA | Start Date*: 2016-06-24 | |||||||||||
Sponsor Name:Krka, d.d., Novo mesto | |||||||||||||
Full Title: Efficacy and Safety of Prolonged Release (SR) Tramadol Hydrochloride (HCl)/Paracetamol fixed combination and Immediate Release (IR) Tramadol HCl/Paracetamol fixed combination in Patients with Moder... | |||||||||||||
Medical condition: Moderate to severe acute low-back pain (12 weeks or less of symptoms). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) CZ (Completed) HR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005259-28 | Sponsor Protocol Number: LCAT | Start Date*: 2016-02-22 | ||||||||||||||||
Sponsor Name:LUMC | ||||||||||||||||||
Full Title: A randomized, double blind, placebo-controlled study on the effect of 3 months treatment with the analgesic tapentadol on conditioned pain modulation (CPM) and pain relief in patients with chronic ... | ||||||||||||||||||
Medical condition: Low back pain | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005495-34 | Sponsor Protocol Number: A4091059 | Start Date*: 2016-01-25 | |||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 3, RANDOMIZED, DOUBLE BLIND, PLACEBO AND ACTIVE-CONTROLLED, MULTICENTER, PARALLEL-GROUP STUDY OF THE ANALGESIC EFFICACY AND SAFETY OF TANEZUMAB IN ADULT SUBJECTS WITH CHRONIC LOW BACK PAIN | |||||||||||||
Medical condition: CHRONIC LOW BACK PAIN | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) DK (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004530-29 | Sponsor Protocol Number: BECRO/WM/PAIN | Start Date*: 2018-01-23 | |||||||||||
Sponsor Name:WinMedica SA | |||||||||||||
Full Title: A Randomized, Multicentre, Double-blind, two Parallel Group, Clinical Phase III Trial for Comparing the Efficacy and Tolerability of a combination IM product of Thiocolchicoside and Diclofenac vs. ... | |||||||||||||
Medical condition: Acute low back pain (LBP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013268-38 | Sponsor Protocol Number: FLUPI-7018 | Start Date*: 2009-09-29 | |||||||||||
Sponsor Name:AWD.pharma GmbH & Co KG | |||||||||||||
Full Title: A multicentre, double-blind, randomised, active- and placebo-controlled clinical trial on the pain relieving effects of the modfied-release formulation of flupirtine in patients suffering from mode... | |||||||||||||
Medical condition: chronic low back pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001920-36 | Sponsor Protocol Number: KF6005/06 | Start Date*: 2012-09-21 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: Efficacy, safety, and tolerability of GRT6005 in subjects with moderate to severe chronic low back pain | |||||||||||||
Medical condition: moderate to severe chronic low back pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) SE (Completed) DK (Completed) HU (Completed) FI (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000067-68 | Sponsor Protocol Number: 044(10A)MD20294 | Start Date*: 2021-06-30 | |||||||||||
Sponsor Name:AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. | |||||||||||||
Full Title: Efficacy and safety of different dosage regimens of the combination methocarbamol/paracetamol in acute Low Back Pain (LBP): MioPain study | |||||||||||||
Medical condition: Acute non-specific Low Back Pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
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: 2009-010428-25 | Sponsor Protocol Number: KF5503/45 | Start Date*: 2010-02-15 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: An evaluation of the effectiveness and tolerability of tapentadol hydrochloride prolonged release, and tapentadol hydrochloride immediate release on demand, in subjects with severe chronic nocicept... | |||||||||||||
Medical condition: Low back Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) NL (Completed) DE (Completed) FR (Completed) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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