- 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 2 of 59.
EudraCT Number: 2012-000730-19 | Sponsor Protocol Number: HEEL-2011-02 | Start Date*: 2012-08-23 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: The analgesic efficacy of Δ9-THC (Namisol®) in Chronic Pancreatitis Patients Suffering From Persistent Abdominal Pain: a Randomized, Double-blinded, Placebo-controlled, Parallel Design | |||||||||||||
Medical condition: Chronic pancreatitis with persistant abdominal pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004918-32 | Sponsor Protocol Number: Study No.: 960 | Start Date*: 2006-04-11 | |||||||||||
Sponsor Name:Biotest AG | |||||||||||||
Full Title: A monocentre, open-label, prospective study investigating the effects of the human normal immunoglobulin Intratect®/ BT 681 for intravenous administration on clinical efficacy, safety, and laborato... | |||||||||||||
Medical condition: Chronic idiopathic pain syndromes (fibromyalgia, myofascial pain, complex regional pain syndrome) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006184-70 | Sponsor Protocol Number: PM07/8404 | Start Date*: 2009-01-09 |
Sponsor Name:The Leeds Teaching Hospitals NHS Trust | ||
Full Title: A POPULATION STUDY INTO THE PREVALENCE AND GENETIC PROFILE OF PATIENTS WITH CHRONIC PAIN WHO DO NOT RESPOND TO ORAL CODEINE A single site, pilot population study into the prevalence and genetic p... | ||
Medical condition: Chronic pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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: 2013-004709-17 | Sponsor Protocol Number: MP_SM01_2013 | Start Date*: 2014-02-10 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of High-dose Naloxone Infusion on Pain and Hyperalgesia in Inguinal Post-herniotomy Patients – A Randomized, Placebo-controlled, Double-blind Study | |||||||||||||
Medical condition: First degree burn injury in healthy volunteers who 6-8 weeks prior have had done a Inguinal herniotomy . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006176-30 | Sponsor Protocol Number: NW-1029/01-08 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:Newron Pharmaceuticals S.p.A. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF TWO FIXED DOSES (160 OR 320 MG/DAY) OF RALFINAMIDE IN PATIENTS WITH CHRONIC NEUROPATHIC LOW BACK PAIN. A MULTICENTER, DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED 12- WEEK ST... | |||||||||||||
Medical condition: Chronic neuropathic low back pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Completed) IT (Completed) GB (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: 2011-000647-24 | Sponsor Protocol Number: HEEL-2011-01 | Start Date*: 2011-07-26 | ||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
Full Title: The safety, tolerability, and analgesic efficacy of Δ9-THC (Namisol®) in chronic pancreatitis patients suffering from persistent abdominal pain | ||||||||||||||||||
Medical condition: patients with abdominal pain as a result of chronic pancreatitis | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2006-005668-21 | Sponsor Protocol Number: NL0605 | Start Date*: 2007-03-22 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare International Limited | |||||||||||||
Full Title: A randomised, double-blind, parallel group, multiple-dose 3 month study of ibuprofen 400mg alone, paracetamol (acetaminophen) 1000mg alone, ibuprofen 200mg plus paracetamol 500mg and ibuprofen 400m... | |||||||||||||
Medical condition: Pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010188-18 | Sponsor Protocol Number: 26859 | Start Date*: 2010-07-01 |
Sponsor Name:Eli Lilly Nederland | ||
Full Title: Effectiveness of Transmural Collaborative care and Duloxetine for major depressive disorder and (sub)chronic pain: a randomized placebo-controlled Multi-Centre trial. | ||
Medical condition: Major depressive disorder (episode or recurrent), as principal DSM-IV diagnosis combined with (sub)chronic pain symptoms as defined bij score of >3 on BPI painlist for at least six weeks. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000992-28 | Sponsor Protocol Number: KCT04/2015-DORETAonko/SI | Start Date*: 2015-07-15 | |||||||||||
Sponsor Name:Krka, d.d., Novo mesto | |||||||||||||
Full Title: A comparison of the severity of acute pain and the frequency of chronic pain after post-operative analgesia of lower and higher intensity following surgical emptying of the axillary gland in breast... | |||||||||||||
Medical condition: Acute pain after surgical emptying of the axillary gland in breast cancer patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005506-32 | Sponsor Protocol Number: Dulo2006 | Start Date*: 2007-03-05 | |||||||||||
Sponsor Name:Danish Pain Research Center | |||||||||||||
Full Title: Pain, anxiety and depression in neuropathic and non-neuropathic pain: Effect of monoamine modulation. | |||||||||||||
Medical condition: Chronic pain: neuropathic pain and fibromyalgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001669-16 | Sponsor Protocol Number: 80-83600-98-3143 | Start Date*: 2015-12-21 |
Sponsor Name:Erasmus MC | ||
Full Title: Duloxetine for chronic osteoarthritis pain; an important alternative? | ||
Medical condition: osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (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: 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: 2015-002694-37 | Sponsor Protocol Number: 507A011 | Start Date*: 2016-09-01 |
Sponsor Name:Kuopio University hospital | ||
Full Title: Dexmedetomidine infusion in pain management during low back surgery Dexmedetomidine is an alpha-2-adrenergic agonist that is used mainly for sedation in the intensive care unit. Alpha-2-adre... | ||
Medical condition: Low back pain, Discus prolapse, Spinal stenosis | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-000944-41 | Sponsor Protocol Number: FenS-FenD | Start Date*: 2015-04-20 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: A PILOT STUDY TO TEST THE FEASIBILITY OF A TWO-ARM, DOUBLE BLIND, PARALLEL-GROUP, RANDOMIZED CONTROLLED TRIAL FOR THE COMPARISON OF THE DURATION OF THE ANALGESIC EFFICACY OF A SINGLE MATRIX TRANSDE... | |||||||||||||
Medical condition: Patients with oncological pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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 |
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