- Trials with a EudraCT protocol (162)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
162 result(s) found for: Oxycodone.
Displaying page 6 of 9.
EudraCT Number: 2019-001861-33 | Sponsor Protocol Number: P19.050 | Start Date*: 2019-07-17 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Cannabis-opioid interaction in the treatment of fibromyalgia pain – an open label proof-of-concept study | ||
Medical condition: Chronic fibromyalgia pain | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003238-15 | Sponsor Protocol Number: Schaefers0711 | Start Date*: 2012-12-12 | |||||||||||
Sponsor Name:KKRN Katholisches Klinikum Ruhrgebiet Nord GmbH | |||||||||||||
Full Title: Quality of analgesia and side effect incidence and severity during postoperative pain management with Palexia® compared to Targin® | |||||||||||||
Medical condition: Management of postoperative pain in trauma surgery patients (adults) requiring postoperative opiates for the management of postoperative pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001951-36 | Sponsor Protocol Number: HTG-Oxy1 | Start Date*: 2006-05-15 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Perioperative Analgesie in der Gefäßchirurgie | ||
Medical condition: peripheral vascular disease, inclusion criteria: elective vascular surgery, age 30 to100years; male and female; exclusion Criteria: amaurosis, insufficient language skills, permanent opioid medicat... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-000140-15 | Sponsor Protocol Number: Neu-rls2014 | Start Date*: 2015-02-24 | |||||||||||
Sponsor Name:Fondazione Neureca Onlus | |||||||||||||
Full Title: Comparative Polysomnographic Study of Oxycodone/Naloxone or Pramipexole for the Treatment of Restless Legs Syndrome | |||||||||||||
Medical condition: Restless legs syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001824-13 | Sponsor Protocol Number: OXIS | Start Date*: 2022-09-12 | ||||||||||||||||
Sponsor Name:Leiden University Medical Center | ||||||||||||||||||
Full Title: Influence of oxycodone on individuals taking an SSRI | ||||||||||||||||||
Medical condition: Depression | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
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: 2006-002087-26 | Sponsor Protocol Number: FT-019-IM | Start Date*: 2006-12-22 | |||||||||||
Sponsor Name:Nycomed Danmark ApS | |||||||||||||
Full Title: An open label, comparative, randomised, balanced crossover trial comparing nasal fentanyl and oral transmucosal fentanyl (Actiq) in breakthrough pain in patients with cancer. | |||||||||||||
Medical condition: Breakthrough pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) IT (Completed) AT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003925-23 | Sponsor Protocol Number: PIANISSIMO | Start Date*: 2023-04-12 |
Sponsor Name:Vrije Universiteit Brussel | ||
Full Title: Pain medication tapering for patients with Persistent Spinal Pain Syndrome Type II, treated with Spinal Cord Stimulation. | ||
Medical condition: Persistent spinal pain syndrome type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003249-34 | Sponsor Protocol Number: F13640GE209 | Start Date*: 2007-09-24 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Proof of Concept study of the efficacy and tolerability of a 4-week treatment with F13640 in patients in whom the adaptation of opioid therapy of cancer pain has failed. A prospective, multinationa... | |||||||||||||
Medical condition: Patients who have failed adaptation of opioid therapy for cancer pain | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013329-41 | Sponsor Protocol Number: A4091030 | Start Date*: 2010-01-12 | ||||||||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | ||||||||||||||||||
Full Title: ESTUDIO EN FASE III, MULTICÉNTRICO, ALEATORIZADO, DOBLE CIEGO Y CONTROLADO CON PLACEBO Y OXICODONA PARA DETERMINAR LA EFICACIA Y LA SEGURIDAD DE TANEZUMAB EN PACIENTES CON ARTROSIS DE RODILLA O CAD... | ||||||||||||||||||
Medical condition: ARTROSIS DE RODILLA Y CADERA osteoarthritis of the knee and hip | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) SE (Completed) DE (Completed) AT (Completed) DK (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011774-15 | Sponsor Protocol Number: BASt01 | Start Date*: 2009-07-15 | |||||||||||||||||||||
Sponsor Name:Federal Highway Research Institute / Bundesanstalt für Straßenwesen (BASt) | |||||||||||||||||||||||
Full Title: Effects of opioid analgesics on driving ability of pain patients [Untersuchung zur Fahrsicherheit von Schmerzpatienten] | |||||||||||||||||||||||
Medical condition: patients suffering from chronic non-cancer pain responsive to opioid analgesics under already existing long-term treatment | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021017-23 | Sponsor Protocol Number: STUDIO CERP | Start Date*: 2010-10-20 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: RCT comparing the analgesic efficacy of 4 therapeutic strategies based on 4 different major opioids (fentanyl, oxycodone, buprenorphine vs morphine) in cancer patients with moderate/severe pain, at... | |||||||||||||
Medical condition: Cancer patients with locally advanced or metastatic solid tumor. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002292-27 | Sponsor Protocol Number: NonOnco2008 | Start Date*: 2008-06-23 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Long term opioid administration in no-oncologic chronic pain: open label, prospective study on efficacy, safety and pharmacokinetic factors | |||||||||||||
Medical condition: chronic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002273-12 | Sponsor Protocol Number: Onco2008 | Start Date*: 2008-06-23 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Long term opioid administration in oncologic chronic pain: open label, prospective study on efficacy, safety and pharmacogenetic factors. | |||||||||||||
Medical condition: oncologic chronic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004527-19 | Sponsor Protocol Number: LAL1 | Start Date*: 2006-01-30 |
Sponsor Name:MRC Health Services Research Collaboration | ||
Full Title: Joint pain personalised treatment assessment to investigate the acceptability of modified release oxycontin for managing chronic pain in patients with osteoarthritis of the hip | ||
Medical condition: Hip Osteoarthritis | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-010539-41 | Sponsor Protocol Number: 21428 | Start Date*: 2009-03-23 | |||||||||||
Sponsor Name:Vejle Sygehus | |||||||||||||
Full Title: Norspan versus Oxycontin som postoperativ smertebehandling til ekstracapsulære femurfraktur. Et randomiseret, dobbelt-blindet og placebo-kontrolleret pilotstudium. | |||||||||||||
Medical condition: Norspan versus Oxycontin som postoperativ smertebehandling til ekstracapsulære femurfrakturer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000419-42 | Sponsor Protocol Number: Nalogexol-2014 | Start Date*: 2015-05-11 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: Naloxegol and assessments of opioid induced bowel dysfunction | |||||||||||||
Medical condition: Healthy volunteers (Opioid-induced bowel dysfunction) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005393-31 | Sponsor Protocol Number: CL_700_015_PRO | Start Date*: 2008-08-25 |
Sponsor Name:Akela Pharma Inc | ||
Full Title: A Multicenter, Multinational, Randomized, Double-Blind, Placebo-Controlled, Cross-Over Trial to Evaluate Efficacy and Safety of Fentanyl TAIFUN® Treatment after Titrated Dose Administration for Bre... | ||
Medical condition: Breakthrough pain in opioid tolerant cancer patients. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) CZ (Completed) HU (Completed) BG (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004796-39 | Sponsor Protocol Number: PT-SM-14-OA | Start Date*: 2013-04-30 | ||||||||||||||||
Sponsor Name:Fondazione IRCCS Policlinico San Matteo | ||||||||||||||||||
Full Title: A Comparative Study of Oxycodone/Naloxone versus Codeine/Paracetamol in the Treatment of Moderate to Severe Chronic Knee and/or hip Pain Due to Osteoarthritis | ||||||||||||||||||
Medical condition: Moderate to Severe Chronic Knee and/or hip Pain Due to Osteoarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004609-26 | Sponsor Protocol Number: Methadone-FR-CL0390 | Start Date*: 2011-12-02 | |||||||||||
Sponsor Name:Laboratoires Bouchara-Recordati | |||||||||||||
Full Title: Evaluation of the efficacy and safety of two methadone titration methods for the treatment of cancer-related pain with inadequate pain relief or intolerable side effects when treated with level 3 o... | |||||||||||||
Medical condition: Treatment of cancer-related-pain in patients with inadequate pain relief or intolerable side effects when treated with level 3 opioid. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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