- Trials with a EudraCT protocol (1,162)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
1,162 result(s) found for: Chronic Pain.
Displaying page 8 of 59.
EudraCT Number: 2009-012713-22 | Sponsor Protocol Number: version 28.10.2009 | Start Date*: 2010-05-06 |
Sponsor Name:Medizinische Universität Wien, Univ. Klinik für Anästhesie, Allg. Intensivmedizin u Schmerztherapie | ||
Full Title: Randomized Double-blind Study Comparing the Efficacy of Duloxetine with Placebo in Patients with Chronic Low Back Pain | ||
Medical condition: efficacy of duloxetine in the treatment of patients with chronic low back pain to placebo | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (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: 2008-008235-28 | Sponsor Protocol Number: 82772673 | Start Date*: 2009-01-28 | |||||||||||
Sponsor Name:Vesa Pakanen | |||||||||||||
Full Title: Parasetamolin käyttö oheiskipulääkkeenä oksikodonin kanssa ohitusleikkauksen jälkeisen kivun hoidossa Paracetamol as Adjuctive Treatment for Postoperative Pain after Off-Pump Bypass Surgery | |||||||||||||
Medical condition: Patient with chronic ischemic heart disease ongoing elective coronary artery bypass grafting. Any major organ failures like heart, kidney, liver failures are excluded. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-006196-12 | Sponsor Protocol Number: 160374 | Start Date*: 2006-06-05 |
Sponsor Name:Nottingham City Hospital NHS Trust | ||
Full Title: Epidural steroid injection in chronic, lumbar back pain; a cross-over, single-blinded study of Methyl-prednisolone 80mg versus Methyl-prednisolone 40mg. | ||
Medical condition: Chronic, lumbar back pain. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004951-34 | Sponsor Protocol Number: RESP301-005 | Start Date*: 2020-12-11 | ||||||||||||||||
Sponsor Name:Thirty Respiratory Limited | ||||||||||||||||||
Full Title: Community participants with COPD or bronchiectasis and at risk of Respiratory Viral Infections including SARS-CoV-2: An open-label, multicentre feasibility study of an inhaled nitric oxide generati... | ||||||||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) and bronchiectasis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
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: 2013-002774-51 | Sponsor Protocol Number: BrePainGenOxyc1 | Start Date*: 2013-06-27 |
Sponsor Name:Helsinki University Central Hospital | ||
Full Title: Genetic influences on pain and oxycodone consumption following mastectomy | ||
Medical condition: Women who are scheduled for breast cancer surgery. | ||
Disease: | ||
Population Age: | Gender: | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
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: 2015-000550-37 | Sponsor Protocol Number: NL52444.058.15 | Start Date*: 2015-04-01 |
Sponsor Name:LUMC | ||
Full Title: Effect of Sodium NItroprusside (SNP) on R,S- and S-Ketamine-induced psychotropic side effects, hemodynamic changes and pain relief in healthy volunteers | ||
Medical condition: Chronic pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001656-21 | Sponsor Protocol Number: KF0151Y/06 | Start Date*: 2005-08-11 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: A randomized, multi-center, double-blind, parallel-group, multiple-dose study assessing the analgesic efficacy and safety of 3 different doses of GRT0151Y compared to placebo and an active comparat... | |||||||||||||
Medical condition: Postoperative pain following tonsillectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) CZ (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000642-22 | Sponsor Protocol Number: SEMG | Start Date*: 2017-07-19 |
Sponsor Name:Jose Alberola-Rubio | ||
Full Title: Electromyographic study for the help and guidance of Botox administration in the treatment of chronic pelvic floor pain | ||
Medical condition: Chronic pelvic pain | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003930-10 | Sponsor Protocol Number: KEKU1 | Start Date*: 2018-01-12 |
Sponsor Name:Recherche et enseignement en douleur, anesthesie reanimation | ||
Full Title: KETAMINE'S EFFICIENCY IN THE TREATMENT OF CHRONIC PAIN WITH INFLAMMATORY COMPONENT: EXPLORING THE KYNURENIN PATHWAYS. A controlled, placebo-controlled, double-blind trial. | ||
Medical condition: The population selected is a spinal cord injury population with central neuropathic pain at the lesional or sub-lesion level, chronically (for more than three months) Adult, spinal cord injury (SCI... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015840-40 | Sponsor Protocol Number: LEVO/HK | Start Date*: 2009-10-19 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: Chronic pain and mobility outcomes following primary hip arthroplasty. A comparison of intravenous morphine with lumbar plexus levobupivacaine. | ||
Medical condition: Acute and chronic pain following hip replacement surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-005061-20 | Sponsor Protocol Number: ONU3705 | Start Date*: 2012-06-19 | ||||||||||||||||
Sponsor Name:Purdue Pharma L.P. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Double-dummy, Placebo-controlled, Active-controlled, Parallel-group, Multicenter Trial of Oxycodone/Naloxone Controlled-release Tablets (OXN) to Assess the Analgesic Eff... | ||||||||||||||||||
Medical condition: Opioid-induced Constipation & Moderate to Severe Chronic Low back Pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) PL (Completed) SK (Completed) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002616-13 | Sponsor Protocol Number: Unknown | Start Date*: 2018-03-14 |
Sponsor Name:Maastricht Universitair Medisch Centrum | ||
Full Title: The effect of perioperative intravenous s-ketamine on acute and chronic postoperative craniotomy pain compared to placebo | ||
Medical condition: Post operative craniotomy pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003688-24 | Sponsor Protocol Number: P12.??? | Start Date*: 2012-12-12 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Treatment of Complex Regional Pain Syndrome type 1: A randomized placebo controlled double-blind study with ARA 290 | ||
Medical condition: Complex regional pain syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000906-12 | Sponsor Protocol Number: AQX-1125-301 | Start Date*: 2016-09-07 | ||||||||||||||||
Sponsor Name:Aquinox Pharmaceuticals (Canada) Inc. | ||||||||||||||||||
Full Title: The LEADERSHIP 301 Trial: A 12-Week, Randomized, Multi-Center, Double-Blind, Placebo-Controlled, 3 Arm, Parallel-Group, Phase 3 Trial to Evaluate the Efficacy and Safety of 2 Doses of AQX-1125 Targ... | ||||||||||||||||||
Medical condition: Interstitial Cystitis/Bladder Pain Syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) HU (Completed) CZ (Completed) LV (Prematurely Ended) GB (Prematurely Ended) BE (Completed) ES (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003972-21 | Sponsor Protocol Number: DS5565-A-U307 | Start Date*: 2015-09-10 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED SAFETY STUDY OF DS-5565 FOR TREATMENT OF PAIN DUE TO FIBROMYALGIA IN SUBJECTS WITH CHRONIC KIDNEY DISEASE | |||||||||||||
Medical condition: DS-5565 is being investigated for the treatment of pain associated with fibromyalgia (FM) in subjects with chronic kidney disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) BG (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: 2011-002143-95 | Sponsor Protocol Number: M12-141 | Start Date*: 2012-10-04 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo- and Active-Controlled Study Comparing the Safety and Analgesic Efficacy of ABT-110 to Placebo in 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: NO (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
Trial results: View results |
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