- Trials with a EudraCT protocol (1,163)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,163 result(s) found for: Chronic Pain.
Displaying page 5 of 59.
| EudraCT Number: 2012-005499-33 | Sponsor Protocol Number: HP5503-88 | Start Date*: 2014-11-11 | |||||||||||
| Sponsor Name:Grünenthal GmbH | |||||||||||||
| Full Title: Relative bioavailability trial to investigate the pharmacokinetics of tapentadol following the administration of 3 prototype tapentadol 25 mg prolonged release (PR) granule formulations compared to... | |||||||||||||
| Medical condition: No medical condition to be investigated. | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004612-19 | Sponsor Protocol Number: IIBSP-COR-2017-98 | Start Date*: 2018-03-20 |
| Sponsor Name:Institut de Recerca Hospital de la Santa Creu i Sant Pau | ||
| Full Title: EFFICACY OF THE SUPRAESCAPULAR NERVE APPROACH WITH CORTICOIDS ADMINISTRATION VERSUS PULSED RADIOFREQUENCY IN CHRONIC SHOULDER PAIN. DOUBLE BLIND RANDOMIZED CLINICAL TRIAL | ||
| Medical condition: Chronic shoulder pain | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005365-11 | Sponsor Protocol Number: KF5303/01 | Start Date*: 2006-03-31 |
| Sponsor Name:Grünenthal GmbH | ||
| Full Title: A randomised, 2-arm, parallel group study assessing efficacy and tolerability of titrated transdermal buprenorphine in patients with moderate to severe chronic non malignant pain | ||
| Medical condition: Moderate to severe chronic pain | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) AT (Completed) HU (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002266-71 | Sponsor Protocol Number: GN14RE146 | Start Date*: 2015-01-02 | |||||||||||
| Sponsor Name:NHS Greater Glasgow and Clyde | |||||||||||||
| Full Title: The role of Qutenza (topical capsaicin 8%) in treating neuropathic pain from arteriovenous fistulae in patients with end stage renal failure | |||||||||||||
| Medical condition: Chronic neuropathic pain from arteriovenous fistulae in patients with end stage renal failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-003752-19 | Sponsor Protocol Number: OXN3401 | Start Date*: 2005-02-01 | |||||||||||
| Sponsor Name:Mundipharma Research GmbH & Co.KG | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo- and Active-controlled, Double-dummy, Parallel Group Study to Determine the Safety and Efficacy of Oxycodone/Naloxone Prolonged-release Tablets in Subjects with ... | |||||||||||||
| Medical condition: Moderate to severe chronic pain of low back that requires around-the-clock opioid therapy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) DK (Completed) SK (Completed) ES (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004255-38 | Sponsor Protocol Number: cnp-MS-0601/MC-2006-01 | Start Date*: 2007-01-05 | |||||||||||
| Sponsor Name:Bionorica research GmbH | |||||||||||||
| Full Title: Multi-centre, randomized, double-blind, placebo-controlled study to investigate the efficacy and safety of the pain relieving effect of Dronabinol in patients with multiple sclerosis associated wit... | |||||||||||||
| Medical condition: Patients with multiple sclerosis associated with central neuropathic pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) DK (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003430-16 | Sponsor Protocol Number: OC004PDS | Start Date*: 2012-11-15 | |||||||||||
| Sponsor Name:Clinical Reasearch Centre, Hvidovre University Hospital | |||||||||||||
| Full Title: Effect of local anesthesia in patients with marginal periodontitis undergoing subgingival scaling | |||||||||||||
| Medical condition: Pain and discomfort during dental treatment in patients with periodontitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001985-34 | Sponsor Protocol Number: KF5503/16/ R331333-PAI-3014 | Start Date*: 2008-02-15 | ||||||||||||||||
| Sponsor Name:& Johnson Pharmaceutical Research & Development, L.L.C. | ||||||||||||||||||
| Full Title: A randomized withdrawal, active- and placebo-controlled, double-blind, multi-center Phase III trial assessing safety and efficacy of oral CG5503 PR* in subjects with moderate to severe chronic mali... | ||||||||||||||||||
| Medical condition: The treatment of chronic tumor-related pain. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: LV (Prematurely Ended) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-000793-36 | Sponsor Protocol Number: HighNxGHR | Start Date*: 2015-04-28 | |||||||||||
| Sponsor Name:Rigshospitalet, Copenhagen University Hospitals | |||||||||||||
| Full Title: Effect of High-dose Target-controlled Naloxone Infusion on Pain and Hyperalgesia in Patients following Groin-Hernia-Repair. A companion study to: Pharmacokinetics of High-dose Target-controlled Nal... | |||||||||||||
| Medical condition: Groin hernia repair | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002177-35 | Sponsor Protocol Number: GNB-2015 | Start Date*: 2018-05-07 |
| Sponsor Name:Masarykova univerzita | ||
| Full Title: The effect of gabapentin used as a preemptive to the emergence and development chronic neuropathic pain in patients after spinal cord trauma | ||
| Medical condition: Chronic neuropathic pain in patients after spinal cord trauma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-006147-25 | Sponsor Protocol Number: UTEROXINE | Start Date*: 2022-11-15 | |||||||||||||||||||||||||||||||
| Sponsor Name:Centre de Recherche en Santé de la Femme | |||||||||||||||||||||||||||||||||
| Full Title: Botulinum toxin type A injection in patients with chronic pelvic pain of uterine origin (severe dysmenorrhea and/or deep dyspareunia). Phase III, single-center, randomized study vs. control group | |||||||||||||||||||||||||||||||||
| Medical condition: PATIENTS WITH CHRONIC PELVIC PERINEAL PAIN OF UTERINE ORIGIN WITH VAS>4 | |||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2006-003482-14 | Sponsor Protocol Number: KF5503/24-R331333-PAI-3007 | Start Date*: 2007-02-23 | |||||||||||
| Sponsor Name:Johnson & Johnson Pharamceutical Resarch & Development, L.L.C | |||||||||||||
| Full Title: A One-Year, Randomized, Open-Label, Parallel-Arm, Phase III Long-Term Safety Trial, with Controlled Adjustment of Dose, of Multiple Doses of CG5503 PR* and Oxycodone CR in Subjects with Chronic Pain | |||||||||||||
| Medical condition: Chronic pain due to knee or hip osteoarthritis or low back pain of benign origin | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) NL (Completed) AT (Completed) BE (Completed) GB (Completed) SK (Completed) SI (Prematurely Ended) FR (Completed) CZ (Completed) DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004779-64 | Sponsor Protocol Number: ALMED-15-C2-054 | Start Date*: 2016-12-20 | |||||||||||
| Sponsor Name:Air Liquide Santé International | |||||||||||||
| Full Title: Equimolar Mixture of Oxygen and Nitrous Oxide (EMONO) for the Treatment of Peripheral Neuropathic Pain: a Randomised, International, Multicentre, Placebo-Controlled, Phenotype-stratified Phase IIa ... | |||||||||||||
| Medical condition: Treatment Peripheral Neuropathic Pain | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) FR (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: 2011-004555-39 | Sponsor Protocol Number: 3652-CL-0018 | Start Date*: 2012-05-07 | ||||||||||||||||||||||||||
| Sponsor Name:Astellas Pharma Europe B.V. | ||||||||||||||||||||||||||||
| Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel group, Adaptive, combined Proof of Concept and Dose-Finding study to investigate Efficacy, Safety, Pharmacodynamics and Pharmacokin... | ||||||||||||||||||||||||||||
| Medical condition: Bladder Pain Syndrome / Interstitial Cystitis | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) NL (Completed) CZ (Completed) DE (Completed) LV (Completed) PT (Completed) ES (Completed) PL (Completed) DK (Completed) LT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2015-001523-24 | Sponsor Protocol Number: 14744001 | Start Date*: 2016-03-25 | |||||||||||
| Sponsor Name:UHToulouse | |||||||||||||
| Full Title: Evaluation of the analgesic effects of prolonged-release oxycodone and of L-Dopa, versus placebo, on central neuropathic pain in Parkinson's disease : OXYDOPA trial | |||||||||||||
| Medical condition: Central neuropathic pain in Parkinson's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-003171-21 | Sponsor Protocol Number: LEV-2005 | Start Date*: 2005-11-02 |
| Sponsor Name:Danish Pain Research Center | ||
| Full Title: Effect of levetiracetam in spinal cord injury pain: a randomized, double-blind, placebo-controlled crossover study | ||
| Medical condition: Neuropathic pain following spinal cord injury | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-003379-28 | Sponsor Protocol Number: 0663-098 | Start Date*: 2009-03-11 | |||||||||||
| Sponsor Name:Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase III Randomized, Double-Blind, Placebo- and Active-Comparator-Controlled, Multiple-Dose, Clinical Trial to Study the Safety and Efficacy of MK-0663/Etoricoxib and Ibuprofen in the Treatment ... | |||||||||||||
| Medical condition: Pain after total knee replacement | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) LT (Completed) EE (Completed) HU (Completed) SI (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: 2006-006958-10 | Sponsor Protocol Number: 01/06/57 | Start Date*: 2007-09-26 |
| Sponsor Name:Pharmanord, UK, LTD | ||
| Full Title: Anticipate Trial - Randomized, Double blind, placebo-controlled, multicentre Trial of Anti-oxidant therapy in painful chronic pancreatitis. | ||
| Medical condition: Chronic Pancreatitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
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