- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
74 result(s) found for: Chronic Low Back Pain.
Displaying page 1 of 4.
| 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: 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: 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: 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: 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: 2012-001920-36 | 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: 2013-004564-55 | Sponsor Protocol Number: COSTAL-2013 | Start Date*: 2014-03-10 | |||||||||||
| Sponsor Name:MEDITOP Gyógyszeripari Kft | |||||||||||||
| Full Title: A randomized, multicenter, double-blind, placebo controlled, parallel study to assess the efficacy and safety of the combined administration of sertraline and lamotrigine in subjects with chronic l... | |||||||||||||
| Medical condition: Chronic low back pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) RO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | |||||||||||||
| EudraCT Number: 2012-002943-11 | Sponsor Protocol Number: KF5503/60 | Start Date*: 2013-02-25 | ||||||||||||||||
| Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
| Full Title: Evaluation of the effectiveness, safety, and tolerability of tapentadol PR versus oxycodone/naloxone PR in non-opioid pre-treated subjects with uncontrolled severe chronic low back pain with a neur... | ||||||||||||||||||
| Medical condition: Severe chronic low back pain with a neuropathic pain component | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) IT (Completed) AT (Completed) ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-009857-17 | Sponsor Protocol Number: 42160443PAI2003 | Start Date*: 2009-12-16 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging, Dose-Loading Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Inadequate... | |||||||||||||
| Medical condition: Moderate to severe, chronic, low back pain (LBP) that is not adequately controlled by standard pain therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005278-86 | Sponsor Protocol Number: 147(Z)WO20157 | Start Date*: 2021-06-14 | ||||||||||||||||
| Sponsor Name:AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. | ||||||||||||||||||
| Full Title: Efficacy and safety of the combination of ibuprofen and paracetamol versus ibuprofen in monotherapy in acute Low Back Pain (LBP) | ||||||||||||||||||
| Medical condition: Low Back Pain (LBP) | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) PL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-010427-12 | Sponsor Protocol Number: KF5503/44 | Start Date*: 2009-10-14 | |||||||||||
| 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 uncontrolled severe chr... | |||||||||||||
| Medical condition: Low back Pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) FR (Completed) AT (Completed) DE (Completed) IT (Completed) PL (Completed) ES (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: 2006-003484-31 | Sponsor Protocol Number: F1J-MC-HMEN | Start Date*: 2006-12-13 | |||||||||||
| Sponsor Name:Eli Lilly and Company Ltd. | |||||||||||||
| Full Title: Effect of Duloxetine 60 mg to 120 mg Once Daily in Patients with Chronic Low Back Pain | |||||||||||||
| Medical condition: Chronic Low Back Pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) FR (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002248-40 | Sponsor Protocol Number: F1J-MC-HMGC | Start Date*: 2008-08-04 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Effect of Duloxetine 60 mg Once Daily versus Placebo in Patients with Chronic Low Back Pain | |||||||||||||
| Medical condition: Chronic low back pain (CLBP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-000724-37 | Sponsor Protocol Number: EP-DIC-TIO/75+4-F-01-2022 | Start Date*: 2022-11-08 | ||||||||||||||||
| Sponsor Name:EPIFARMA S.R.L. | ||||||||||||||||||
| Full Title: Randomized, double-blind, parallel-groups, active - and placebo-controlled study to Evaluate the efficacy of a fixed combination of diclofenac 75 mg + thiocolchicoside 4 mg as solution for injectio... | ||||||||||||||||||
| Medical condition: Low back pain (LBP) is one of the most frequent and disabling health problems. It is estimated that about 80% of adults will experience an episode of acute or chronic LBP at least once during their... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) GR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-004943-54 | Sponsor Protocol Number: STA-02 | Start Date*: 2020-06-15 | |||||||||||
| Sponsor Name:Stayble Therapeutics AB | |||||||||||||
| Full Title: A multi-country, randomized, double-blind, placebo-controlled study investigating the efficacy and safety of STA363 at two concentrations (60 mg/mL and 120 mg/mL) compared to placebo in patients wi... | |||||||||||||
| Medical condition: Сhronic discogenic low back pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004861-29 | Sponsor Protocol Number: Modic03 | Start Date*: 2018-05-16 | |||||||||||
| Sponsor Name:FOU, Nevroklinikken, Oslo University Hospital -Ullevål | |||||||||||||
| Full Title: BackToBasic: The effect of Infliximab in patients with chronic low back pain and Modic changes. A randomized, double blind, placebo-controlled, multicenter trial | |||||||||||||
| Medical condition: Non-specific chronic low back pain of more than 6 months duration. We will only investigate those who have vertebral end-plate chanages(Modic changes) on MRI. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019998-14 | Sponsor Protocol Number: KF5503/58 | Start Date*: 2011-02-15 | ||||||||||||||||
| Sponsor Name:Grünenthal GmbH | ||||||||||||||||||
| Full Title: Evaluation of the effectiveness, safety, and tolerability of tapentadol PR versus a combination of tapentadol PR and pregabalin in subjects with severe chronic low back pain with a neuropathic pain... | ||||||||||||||||||
| Medical condition: severe chronic low back pain with a neuropathic pain component | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) DE (Completed) AT (Completed) BE (Completed) ES (Completed) DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2004-000487-27 | Sponsor Protocol Number: 0663-806 | Start Date*: 2004-08-10 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
| Full Title: A Double-Blind, Parallel-Group, 4-week Trial to Assess the Efficacy and Safety of Etoricoxib 60mg and Diclofenac 150mg in Patients 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) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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