- Trials with a EudraCT protocol (5,490)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (75)
5,490 result(s) found for: Pain..
Displaying page 9 of 275.
EudraCT Number: 2010-022025-15 | Sponsor Protocol Number: 10-2-055 | Start Date*: 2011-02-21 |
Sponsor Name:MUMC | ||
Full Title: Intradiscal Methylene Blue Injection Treatment for Chronic Discogenic Low back pain A prospective Clinical Series followed by a Randomised Placebo-Controlled Clinical Trial | ||
Medical condition: The Randomized Clinical Trial (RCT) aims to prove the hypothesis that Intradiscal Methylene blue Injection is capable of better pain reduction than the best available treatment in patients sufferin... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000096-36 | Sponsor Protocol Number: Botox-01 | Start Date*: 2021-06-23 | |||||||||||
Sponsor Name:Department of Dermatology and Copenhagen Wound Healing Center, Bispebjerg Hospital | |||||||||||||
Full Title: The effect of subcutaneous injection of Botulinum Toxin A on chronic wound pain in lower extremities, a prospective exploratory study | |||||||||||||
Medical condition: chronic wound pain and wound healing | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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: 2011-003082-15 | Sponsor Protocol Number: KTB-002 | Start Date*: 2011-09-08 | ||||||||||||||||
Sponsor Name:Karen Toftdahl Bjørnholdt | ||||||||||||||||||
Full Title: High dose dexamethasone for pain following arthroscopic shoulder surgery: A randomised blinded clinical trial. | ||||||||||||||||||
Medical condition: Pain following arthroscopic shoulder surgery. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009856-19 | Sponsor Protocol Number: 42160443PAI2004AmINT-2 | Start Date*: 2009-12-17 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 as Adjunctive Therapy in Subjects With Moderate to Severe Knee ... | |||||||||||||
Medical condition: moderate to severe, chronic, knee or hip pain from osteoarthritis (OA) that is not adequately controlled by standard pain therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004341-24 | Sponsor Protocol Number: KCT11/2017–BLOSSOM | Start Date*: 2019-06-28 |
Sponsor Name:Krka, d.d., Novo Mesto | ||
Full Title: Efficacy of pregabalin and duloxetine in patients with painful diabetic peripheral neuropathy (PDPN): the effect of pain on cognitive function, sleep and quality of life (BLOSSOM) | ||
Medical condition: The purpose of the trial is to assess the efficacy of Pregabalin Krka (pregabalin) and Dulsevia® (duloxetin) in patients with PDPN, investigate the effect of Pregabalin Krka and Dulsevia® on pain a... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) PL (Completed) HR (Completed) | ||
Trial results: View results |
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: 2011-002743-10 | Sponsor Protocol Number: A0081268 | Start Date*: 2012-01-05 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A STUDY OF PREGABALIN IN THE TREATMENT OF SUBJECTS WITH PAINFUL DIABETIC PERIPHERAL NEUROPATHY WITH BACKGROUND TREATMENT OF NSAID FOR OTHER PAIN CONDITIONS | |||||||||||||
Medical condition: PAINFUL DIABETIC PERIPHERAL NEUROPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004181-18 | Sponsor Protocol Number: SM-RS-2012 | Start Date*: 2012-11-23 | |||||||||||
Sponsor Name:Rigshospitalet; Department of Anaesthesia | |||||||||||||
Full Title: The effect of dexamethasone in combination with paracetamol and ibuprofen as adjuvant, postoperative pain after herniated disk surgery | |||||||||||||
Medical condition: Patients set to lumbar prolapse surgery in general anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005656-26 | Sponsor Protocol Number: 51748.094.15 | Start Date*: 2015-10-14 | ||||||||||||||||
Sponsor Name:Westfriesgasthuis | ||||||||||||||||||
Full Title: Amitriptyline 10% and ketamine 10% cream in neuropathic pain: A randomised, double-blind, placebo-controlled cross-over pilot study with a three months open follow-up | ||||||||||||||||||
Medical condition: Patients with peripheral neuropathic pain or scar pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004317-18 | Sponsor Protocol Number: TAP4 | Start Date*: 2009-06-09 | |||||||||||
Sponsor Name:Dept of Anaesthesia, University College Hospital, Galway | |||||||||||||
Full Title: Comparison of continuous Lumbar Epidural (LEP) and Transversus Abdominis Plane (TAP) Blockade in the management of postoperative pain post abdominal surgery. | |||||||||||||
Medical condition: Postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002223-42 | Sponsor Protocol Number: A4091061 | Start Date*: 2015-10-12 | |||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 3 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY OF THE ANALGESIC EFFICACY AND SAFETY OF THE SUBCUTANEOUS ADMINISTRATION OF TANEZUMAB (PF-04383119) IN SUBJECTS WITH CANCER ... | |||||||||||||
Medical condition: Metastatic Bone Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) PL (Completed) ES (Completed) SK (Completed) HU (Completed) RO (Completed) FR (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005886-41 | Sponsor Protocol Number: AUH-PAIN-01 | Start Date*: 2022-06-29 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Efficacy of Perioperative Long-acting Anesthesia by Local Infiltration Following Median Sternotomy - The PAIN Trial | |||||||||||||
Medical condition: Acute postoperative pain after coronary bypass grafting surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004423-20 | Sponsor Protocol Number: V00498TA301 | Start Date*: 2013-01-10 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: STUDY OF EFFICACY AND SAFETY OF V0498 VERSUS PLACEBO IN ACUTE SORE THROAT PAIN | |||||||||||||
Medical condition: Acute sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) LV (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002791-14 | Sponsor Protocol Number: 1707-CL-0011 | Start Date*: 2013-02-14 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled, Phase 2 Study to Assess the Efficacy, Safety, and Dose-Response Relationship of ASP1707 in Subjects with Endometriosis Associated Pelvic Pain for 12 ... | |||||||||||||
Medical condition: endometriosis associated pelvic pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001876-21 | Sponsor Protocol Number: ACT11917 | Start Date*: 2011-11-22 | |||||||||||
Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
Full Title: MULTINATIONAL, MULTICENTER, RANDOMIZED DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY OF EFFICACY AND SAFETY OF SAR292833 ADMINISTRATION FOR 4 WEEKS IN PATIENTS WITH CHRONIC PERIPHERAL NEUR... | |||||||||||||
Medical condition: Neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002240-24 | Sponsor Protocol Number: 214868-007 | Start Date*: 2013-02-28 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study of the Safety and Efficacy of a Single Treatment of AGN-214868 in Patients With Postherpetic Neuralgia | |||||||||||||
Medical condition: Postherpetic Neuralgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
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: 2006-000397-71 | Sponsor Protocol Number: kepp3 | Start Date*: 2006-05-16 |
Sponsor Name:Søren H. Sindrup, Department of Neurology, Odense University Hospital | ||
Full Title: Double-blind, randomised, placebo-controlled trial of levetiracetam for central neuropathic pain in patients with multiple sclerosis | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001201-10 | Sponsor Protocol Number: FEN-PPA-401 | Start Date*: 2004-07-26 | |||||||||||
Sponsor Name:JANSSEN-CILAG | |||||||||||||
Full Title: Comparison of transdermal fentanyl PCA and IV morphine PCA in the management of post-operative pain control. | |||||||||||||
Medical condition: Treatment of moderate to severe post-operative pain in subjects who have undergone an elective major abdominal or orthopaedic surgical procedure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
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