- Trials with a EudraCT protocol (494)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
494 result(s) found for: Pain disorder.
Displaying page 1 of 25.
EudraCT Number: 2012-001587-30 | Sponsor Protocol Number: GU11SU387 | Start Date*: 2013-09-26 | ||||||||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde | ||||||||||||||||||
Full Title: The role of pre-emptive analgesia with Qutenza (topical capsaicin 8%) in preventing neuropathic pain following lower limb amputation: a pilot randomised controlled study | ||||||||||||||||||
Medical condition: Chronic neuropathic pain following limb amputation | ||||||||||||||||||
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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: 2013-002123-41 | Sponsor Protocol Number: anakinrapain1 | Start Date*: 2013-10-21 | |||||||||||
Sponsor Name:Lovisenberg Diaconal Hospital | |||||||||||||
Full Title: Effects of intraarticular IL1-Ra on pain and inflammatory mediators after knee arthroscopy –a double blind, placebo controlled study using microdialysis technique | |||||||||||||
Medical condition: Post operative pain after diagnostic or therapeutic knee arthroscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002217-34 | Sponsor Protocol Number: FITO-01/21 | Start Date*: 2022-07-26 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: Tuscany project to investigate on efficacy and safety of Cannabis phytotherapic preparations for the treatment of Aromatase iNhibitor-induced chronic resistaNt pAin in Breast cancer patIents: a pro... | |||||||||||||
Medical condition: Aromatase iNhibitor-induced chronic resistaNt pAin in Breast cancer patIents | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-018056-42 | Sponsor Protocol Number: URC/2010/01 | Start Date*: 2010-07-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA G. BROTZU | |||||||||||||
Full Title: A phase IV single-centre study to evaluate the topical administration of capsaicin cream (0.075%) as a healthy volunteer model of neuropathic pain. | |||||||||||||
Medical condition: Creation of a healthy volunteer model of neuropathic pain. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005222-69 | Sponsor Protocol Number: NEUROPAIN01 | Start Date*: 2007-07-24 | |||||||||||
Sponsor Name:Associazione Progetto Oncologia UMAN.A | |||||||||||||
Full Title: Randomized phase II trial evaluating the activity and the tolerability of fixed dose of oxycodone and increasing dose of pregabalin versus increasing dose of oxycodone and fixed dose of pregabalin | |||||||||||||
Medical condition: patients affected with cancer and presenting a neuropatic component in their pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006141-12 | Sponsor Protocol Number: Start | Start Date*: 2008-11-14 | |||||||||||
Sponsor Name:UMCG | |||||||||||||
Full Title: Arthrocentesis as initial treatment of arthropathy of the temporomandibular joint | |||||||||||||
Medical condition: Arthropathy of the temporomandibular joint | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002744-40 | Sponsor Protocol Number: HK_EA_02_2014 | Start Date*: 2014-09-23 | |||||||||||
Sponsor Name:Section For Surgical Pathophysiology, Rigshospitalet | |||||||||||||
Full Title: Preoperative intraarticular injection of methylprednisolone, in patients scheduled for total knee-arthroplasty | |||||||||||||
Medical condition: Knee joint arthrosis with hyperalgesia and severe movement related pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017640-13 | Sponsor Protocol Number: Blocchi09 | Start Date*: 2010-04-21 | |||||||||||
Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | |||||||||||||
Full Title: Continuous peripheral block in the pain and ischemic ulcer treatment in arteriopathy patients | |||||||||||||
Medical condition: Arteriophaty patients with ischemic pain and/or ulcers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000312-36 | Sponsor Protocol Number: PTSD-FMS | Start Date*: 2021-05-19 | ||||||||||||||||
Sponsor Name:Henri Laborit Hospital | ||||||||||||||||||
Full Title: Impact of Post-Traumatic Stress Disorder Treatment by Reconsolidation Therapy on Fibromyalgia Syndrome | ||||||||||||||||||
Medical condition: Post-Traumatic Stress Disorder and fibromyalgia syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002131-32 | Sponsor Protocol Number: SP001033 | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:ASSOCIAZIONE ITALIANA PER LO STUDIO DEL DOLORE | |||||||||||||
Full Title: A RANDOMIZED, OPEN COMPARISON BETWEEN PREGABALIN/TRANSDERMAL BUPRENORPHINE AND PREGABALIN/DICLOFENAC IN CHRONIC NEUROPATHIC PAIN PATIENTS | |||||||||||||
Medical condition: PERIPHERAL NEUROPATHIC PAIN DUE TO POST-HERPETIC NEURALGIA OR DIABETIC POLYNEUROPATHY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023883-42 | Sponsor Protocol Number: IGD002 | Start Date*: 2012-03-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA' GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Randomized, double-blind, placebo controlled trial to evaluate the efficacy of high dose intravenous immunoglobulins in diabetic painful polyneuropaty (DPNP)resistant to conventional therapies | |||||||||||||
Medical condition: painful diabetic polyneuropathy resistant to conventional therapies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000347-28 | Sponsor Protocol Number: KF10004/10 | Start Date*: 2012-09-03 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: Efficacy and safety of lidocaine 5% medicated plaster in localized chronic post-operative neuropathic pain | |||||||||||||
Medical condition: moderate to severe localized chronic post-operative neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) ES (Completed) IT (Completed) DK (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023175-26 | Sponsor Protocol Number: P_TPT_2010 | Start Date*: 2011-01-14 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Influence of Tapentadol on endogenous modulation of pain in chronic neuropathic pain patients and healthy volunteers | |||||||||||||
Medical condition: Chronic pain patients/ mhealthy volunteers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000048-32 | Sponsor Protocol Number: 15-062 | Start Date*: 2018-03-01 |
Sponsor Name:RWTH Aachen University/CTC-A | ||
Full Title: Evaluation of the Therapeutic Effects of Testosterone on Pain Perception in case of Chronic Pain Disorder | ||
Medical condition: Patient with persistent somatoform pain disorder (F45.40 or F45.41) should be included into the study. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-001597-16 | Sponsor Protocol Number: none | Start Date*: 2018-07-18 | |||||||||||
Sponsor Name:Sitnikova Victoria | |||||||||||||
Full Title: Efficacy of botulinum toxin in treating temporomandibular disorders | |||||||||||||
Medical condition: Patients are diagnosed TMD (temporomandibular disorder) according to DC/TMD international consortium: myalgia, local myalgia, myofascial pain, myofascial pain with referral. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007967-18 | Sponsor Protocol Number: MK0462-088 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:CASA DI CURA PRIVATA S.RAFFAELE - PISANA | |||||||||||||
Full Title: A Double-Blind, Placebo Crontrolled, Prallel Group Study to Compare the Efficacy of Rizatriptan 10 mg Iyophilized wafer in the Acute Treatment of Migraine in Patients with Unilateral Trigeminal Aut... | |||||||||||||
Medical condition: not applicable | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011009-18 | Sponsor Protocol Number: ALO-FC-001 | Start Date*: 2009-04-20 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI CAGLIARI | ||||||||||||||||||||||||||||
Full Title: Pilot study on the efficacy of IV haloperidol in the treatment of chronic migraine with and without medication overuse | ||||||||||||||||||||||||||||
Medical condition: Chronic migraine with and without medication overuse | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003503-35 | Sponsor Protocol Number: PAINTX | Start Date*: 2020-02-03 |
Sponsor Name:Region Östergötland | ||
Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study of the Effect of Botulinum Toxin A on Patients with Atypical Odontalgia/Persistent Dentoalveolar Pain. | ||
Medical condition: Atypical Odontalgia/Persistent Dentoalveolar Pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006503-15 | Sponsor Protocol Number: STA-LDH01 | Start Date*: 2023-02-23 | |||||||||||||||||||||
Sponsor Name:Stayble Therapeutics | |||||||||||||||||||||||
Full Title: A prospective, randomised, double-blinded, placebo-controlled study investigating the safety and tolerability of STA363 in patients with radiculopathy caused by lumbar disc herniation | |||||||||||||||||||||||
Medical condition: Radiculopathy due to lumbar intervertebral disc herniation | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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