- Trials with a EudraCT protocol (382)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
382 result(s) found for: Pain Measurement.
Displaying page 1 of 20.
EudraCT Number: 2008-007405-37 | Sponsor Protocol Number: 1497/08 | Start Date*: 2009-03-07 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Multicenter, not-for-profit study to evaluate tolerability, safety of tramadol once-a-day in older patients with dementia and difficulty to verbalize | ||||||||||||||||||
Medical condition: Pain in older patients with dementia | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000360-30 | Sponsor Protocol Number: FEPODPara2021-1 | Start Date*: 2021-05-03 |
Sponsor Name:Helsinki University Hospital | ||
Full Title: Determination of serum paracetamol concentration with an electrochemical measurement tool from blood and saliva samples in patients using also other medication. | ||
Medical condition: Patients with any medical condition that requires regular medication and who are undergoing elective surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021406-38 | Sponsor Protocol Number: Finaledition | Start Date*: 2012-08-28 |
Sponsor Name:Mariefreds Vårdcentral | ||
Full Title: EMLA CREAM AS PAIN RELIEF DURING PNEUMOCOCCAL VACCINATION | ||
Medical condition: Pain relief with Emla cream during Pneumococcal vaccination. | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003947-21 | Sponsor Protocol Number: FDS-0114 | Start Date*: 2015-12-16 |
Sponsor Name:FARMAKA Srl | ||
Full Title: ’Dose dependent pain relieving efficacy and local tolerability of diclofenac oromucosal spray in the treatment of sore throat: A multicenter, parallel-group, double-blind, placebo controlled and ra... | ||
Medical condition: moderate or severe sore throat | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008721-29 | Sponsor Protocol Number: KYT62121/2008-01 | Start Date*: 2009-11-19 | |||||||||||
Sponsor Name:Merck Selbstmedikation GmbH | |||||||||||||
Full Title: Double-blind, randomised, multi-centre, placebo-controlled clinical trail to investigate the efficacy and safety of a combination of comfrey root extract plus methyl nicotinate versus a preparation... | |||||||||||||
Medical condition: Acute upper or low back pain as described in the note for guidance on clinical investigation of medical products for treatment of Nociceptive Pain (CPMP/EWP/612/00. Nov. 21, 2002) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000243-27 | Sponsor Protocol Number: BUPROPION2019 | Start Date*: 2019-03-18 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: The effect of bupropion in peripheral neuropathic pain. A randomized, double-blind, placebo-controlled study. | |||||||||||||
Medical condition: Peripheral neuropathic , i.e. painful polyneuropathy, postherpetic neuralgia and pain after nerve injury (traumatic or surgical). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004738-15 | Sponsor Protocol Number: ADO WAD No-of-1 | Start Date*: 2005-02-03 |
Sponsor Name:Karolinska University Hospital, Huddinge | ||
Full Title: Intermittent intravenous adenosine with prolonged pain in the back of the neck with allodynia/dysaesthesia. | ||
Medical condition: Prolonged pain in the neck caused by a whiplash trauma or another muscle injury. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017163-42 | Sponsor Protocol Number: MR2010 | Start Date*: 2010-05-18 |
Sponsor Name:Karolinska Institute | ||
Full Title: Pain modulation in RA – Influence of adalimumab. A randomized, placebo-controlled study using functional magnetic resonance imaging | ||
Medical condition: Rheumatoid arthritis (RA) The overall aim with this project is to investigate central pain mechanisms in RA and healthy controls, and in RA how these are influenced by autonomic neural regulatio... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000647-27 | Sponsor Protocol Number: Ibu19 | Start Date*: 2019-12-18 | ||||||||||||||||
Sponsor Name:Dicofarm S.p.A. | ||||||||||||||||||
Full Title: Evaluation of efficacy and bioavailability of a new pediatric formulation based on ibuprofen lysinate vs ibuprofen in the management of pain in children | ||||||||||||||||||
Medical condition: Pain on an inflammatory basis (otitis and otomastoiditis, adenite, cellulite, arthritis) and post-operative pain | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020380-20 | Sponsor Protocol Number: R331333-PAI2005/KF5503-59 | Start Date*: 2012-03-09 | |||||||||||
Sponsor Name:Janssen Research & Development, L.L.C. | |||||||||||||
Full Title: Open-Label Evaluation of the Pharmacokinetic Profile and Safety of Tapentadol Oral Solution for the Treatment of Postsurgical Pain in Children and Adolescents Aged From 6 to Less Than 18 Years | |||||||||||||
Medical condition: Pain | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003310-40 | Sponsor Protocol Number: 1SPR11002 | Start Date*: 2014-01-27 | |||||||||||
Sponsor Name:Luitpold Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Single Arm, Open Label Study of the Safety, Efficacy, and Pharmacokinetics of SPRIX® (intranasal ketorolac tromethamine) in 0 to 11 year-Old Patients Undergoing Open Surgical Procedures | |||||||||||||
Medical condition: post open surgery pain (incuding but not limited to orthopedic, abdominal, thoracic, plastic/reconstructive, neurologic [spine], or urologic procedures) | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004870-78 | Sponsor Protocol Number: 202100625 | Start Date*: 2022-03-15 |
Sponsor Name:University Medical Centre Groningen | ||
Full Title: Detecting mitochondrial oxygen tension (mitoPO2) as a measure of local tissue oxygenation in patients with various stages of PAD with the Cellular Oxygen Metabolism (COMET) measurement system of Ph... | ||
Medical condition: Peripheral Arterial disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000938-35 | Sponsor Protocol Number: 1SPR11001 | Start Date*: 2013-06-22 | |||||||||||
Sponsor Name:Luitpold Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Single Arm, Open Label Study to compare the Pharmacokinetics, Safety, and Efficacy of SPRIX® (intranasal ketorolac tromethamine) in 12 to 17 Year-Old Patients vs. Adult Patients (18 - 64 Years) U... | |||||||||||||
Medical condition: post open surgery pain (incuding but not limited to orthopedic, abdominal, thoracic, plastic/reconstructive, neurologic [spine], or urologic procedures) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002177-11 | Sponsor Protocol Number: 80-83600-98-20013 | Start Date*: 2015-04-16 |
Sponsor Name:ZonMW GGG | ||
Full Title: Step-down versus step-up analgesics in patients with (sub)acute sciatica in primary care | ||
Medical condition: Patients with (sub)acute sciatica in primary care. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005087-14 | Sponsor Protocol Number: CPP-401 | Start Date*: 2008-11-12 | ||||||||||||||||
Sponsor Name:Centre Paul Papin | ||||||||||||||||||
Full Title: Comparison of 2 morphine administration’s mode using Pump IntraThecal (IDDS)for Analgesia in patients with Cancer pain, resistant to conventional antalgic treatment | ||||||||||||||||||
Medical condition: Patients with intractable cancer pain, either uncontrolled with standard analgesia , or undergoing severe side effects due to analgesia . Patients undergo implantation of a Medtronic intrathecal pu... | ||||||||||||||||||
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Population Age: | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005116-64 | Sponsor Protocol Number: 16092021 | Start Date*: 2021-12-13 | |||||||||||
Sponsor Name:Aarhus University Hospital, Department of Anesthesiology | |||||||||||||
Full Title: Low-dose ketamine as an adjunct to morphine for acute pain in the ED: a randomized, double-blinded, superiority trial | |||||||||||||
Medical condition: Acute pain in the Emergency Department | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010557-12 | Sponsor Protocol Number: Version1.0/Jan2009 | Start Date*: 2012-03-01 | |||||||||||
Sponsor Name:The Pennine Acute Hospitals NHS Trust | |||||||||||||
Full Title: A Single Blind, Randomised, Cross-over Study to Compare the Efficacy of Lidocaine 5% Plasters(Versatis) versus Pregabalin (Lyrica) in the Treatment of Complex Regional Pain Syndrome, Type 1. | |||||||||||||
Medical condition: Complex regional pain syndrome type 1. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001587-31 | Sponsor Protocol Number: A001-2PX | Start Date*: 2005-06-07 |
Sponsor Name:SantoSolve AS | ||
Full Title: | ||
Medical condition: Patients with fibromyalgia diagnosed according to ACR classification (1990) and with chronic pain at defined symmetrical body areas. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004128-38 | Sponsor Protocol Number: 123 | Start Date*: 2006-02-06 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Pregabalin for pain reduction in Critical Limb Ischemia | ||
Medical condition: Peripheral arterial disease - Critical Limb Ischemia (CLI) CLI is the end stage of peripheral arterial disease in the legs and is a onsequence of deteriorating blood flow supply to the lower limbs.... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003258-21 | Sponsor Protocol Number: PDC-01-0205 | Start Date*: 2022-05-19 | |||||||||||
Sponsor Name:Cessatech A/S | |||||||||||||
Full Title: Analgesic Efficacy and Pharmacokinetic-pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 after Impacted Mandibular Third Molar Extraction | |||||||||||||
Medical condition: Healthy male or female participants scheduled for surgical removal of an impacted mandibular third molar, where bone removal is judged to be needed. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
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