- Trials with a EudraCT protocol (436)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (478)
436 result(s) found for: Paracetamol.
Displaying page 2 of 22.
| EudraCT Number: 2015-004217-24 | Sponsor Protocol Number: s58396 | Start Date*: 2015-11-30 |
| Sponsor Name:UZ Leuven | ||
| Full Title: Pharmacokinetic study of paracetamol in patients over 80 years old admitted to an acute geriatric ward | ||
| Medical condition: Pyrexia Pain | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004908-20 | Sponsor Protocol Number: PARAMRI | Start Date*: 2013-12-23 |
| Sponsor Name:UZ Brussel [...] | ||
| Full Title: Cerebral effect of paracetamol measured by f-MRI | ||
| Medical condition: healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003177-14 | Sponsor Protocol Number: IBUPAR-Trial | Start Date*: 2016-04-06 |
| Sponsor Name: | ||
| Full Title: Paracetamol versus ibuprofen in preterm infants with a hemodynamically significant patent ductus arteriosus: a randomized clinical trial. | ||
| Medical condition: Persistent ductus arteriosus haemodynamically significant | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-005086-20 | Sponsor Protocol Number: CHDR1117 | Start Date*: 2011-11-22 |
| Sponsor Name:Centre for Human Drug Research (CHDR) | ||
| Full Title: Effects of paracetamol on nociception in adolescents. | ||
| Medical condition: Nociceptive pain (disorders) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-000923-33 | Sponsor Protocol Number: HepB/APAP/2011 | Start Date*: 2011-07-14 | ||||||||||||||||
| Sponsor Name:Rijksinstituut voor Volksgezondheid en Milieu (RIVM) | ||||||||||||||||||
| Full Title: Effects of paracetamol use on the immune response after hepatitis B vaccination | ||||||||||||||||||
| Medical condition: No medical conditions will be studied. The association between timing of the use of paracetamol during hepatitis B vaccination and the development of an antibody response will be studied in student... | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-000427-26 | Sponsor Protocol Number: | Start Date*: 2009-06-25 |
| Sponsor Name:Queen Victoria Hospital NHS Foundation Trust | ||
| Full Title: A Comparison of Pre−Medication with Oral Paracetamol versus Intravenous Paracetamol Given at Time of Induction for Postoperative Analgesia Following Wisdom Tooth Extraction | ||
| Medical condition: Pain post wisdom tooth extraction | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005575-14 | Sponsor Protocol Number: R-01270-A015 | Start Date*: 2006-08-08 |
| Sponsor Name:Baxter R&D Europe S.C.R.L | ||
| Full Title: A randomized, double-blind, placebo-controlled, single-dose, parallel-group comparison of the analgesic efficacy, safety and local tolerability of intravenous paracetamol 1% solution Bioren (test),... | ||
| Medical condition: Post-surgical dental pain after removal of one or more impacted 3rd mandibular molar(s), associated with moderate to severe pain. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-002226-22 | Sponsor Protocol Number: 2.0 | Start Date*: 2019-04-30 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: The Impact of Target Temperature Management on Drug Metabolism | ||
| Medical condition: Patients after successful cardiopulmonary resuscitation who undergo target temperature management for 24h hours | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000565-36 | Sponsor Protocol Number: 38/2018 | Start Date*: 2018-06-05 |
| Sponsor Name:University of Oulu | ||
| Full Title: Paracetamol and ibuprofen/indomethacin in closing persistent ductus arteriosus | ||
| Medical condition: Patent ductus arteriosus of a premature infant | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000388-10 | Sponsor Protocol Number: WADA_17C09 | Start Date*: 2019-06-11 |
| Sponsor Name:Daniel Sanabria | ||
| Full Title: Clinical trial on the effects of the tramadol and paracetamol on physical, cognitive and brain performance during cycling | ||
| Medical condition: Sports doping | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000197-38 | Sponsor Protocol Number: AC15006 | Start Date*: 2016-08-04 | |||||||||||||||||||||
| Sponsor Name:University of Edinburgh [...] | |||||||||||||||||||||||
| Full Title: A double blind randomised parallel group trial of paracetamol versus placebo in conjunction with strong opioids for cancer related pain. | |||||||||||||||||||||||
| Medical condition: Cancer related pain. | |||||||||||||||||||||||
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| Population Age: Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2020-005123-36 | Sponsor Protocol Number: PARASTOP | Start Date*: 2021-07-05 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: A randomized, double-blind, parallel-group non-inferiority phase III withdrawal trial of paracetamol versus placebo in conjunction with opioids for moderate to severe cancer-related pain | ||
| Medical condition: Adult patients with metastatic cancer disease, cancer-related pain treated with regular strong opioids, receiving paracetamol (1 gram three or four times a day) and with average pain intensity past... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002137-39 | Sponsor Protocol Number: V1 25/07/04 | Start Date*: 2004-09-17 |
| Sponsor Name: | ||
| Full Title: A randomised controlled trial of the combined use of paracetamol and ibuprofen to treat febrile children | ||
| Medical condition: Fevers in childhood not asscoaited with severe disease in the immunocompenetent or fever in the immunocompromised host. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001639-30 | Sponsor Protocol Number: TramaPara8405 | Start Date*: 2006-10-02 |
| Sponsor Name:Department of Anaesthesia&Intensive Care B, Vienna Medical University | ||
| Full Title: Investigation of the antihyperalgesic effect of a combination of tramadol and paracetamol on primary and secondary hyperalgesia in an UV-B induced inflammatory skin pain model in healthy volunteers. | ||
| Medical condition: This is a volunteer study in healthy volunteers. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-014892-31 | Sponsor Protocol Number: MAIVECMOPAIN | Start Date*: 2009-11-10 |
| Sponsor Name:ErasmusMC - Sophia | ||
| Full Title: Morphine intravenous vs. Paracetamol intravenous in children on ECMO | ||
| Medical condition: Patients treated with Extra Corporal Membrane Oxygenation (ECMO) receive morphine as standardised analgesic drug. Morphine is associated with several side effects. In these patients a non-opioid dr... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002213-12 | Sponsor Protocol Number: I10 005 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:CHU de Limoges | ||||||||||||||||||
| Full Title: Paracetamol and setrons : drug interactions in the management of pain after tonsillectomy in children | ||||||||||||||||||
| Medical condition: Pain | ||||||||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-000247-58 | Sponsor Protocol Number: PKZW-NZW201301 | Start Date*: 2013-09-30 |
| Sponsor Name:KU Leuven Departement Ontwikkeling en Regeneratie | ||
| Full Title: Pharmacokinetics of drugs used by pregnant women (paracetamol/macrolide antibiotics): in vivo pharmacokinetic study of pregnant versus non-pregnant women. | ||
| Medical condition: 1) Pregnant women who, due to medical indication, need to take one of the experimental drugs (paracetamol, azithromycin or erythromycin) in the second or third trimester of there pregnancy 2) The s... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004790-10 | Sponsor Protocol Number: A2720382 | Start Date*: 2007-06-06 | |||||||||||
| Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
| Full Title: A Proof-of-Principle Analgesic Adjuvant Pilot Study in Post-Operative Dental Pain | |||||||||||||
| Medical condition: Analgesia induced by dental extraction | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000138-37 | Sponsor Protocol Number: FMLD-HUNGRIA-2-42_FIII | Start Date*: 2018-04-25 |
| Sponsor Name:Laboratorios Farmalíder S.A. | ||
| Full Title: PHASE III CLINICAL TRIAL FOR THE EVALUATION OF THE EFFICACY AND SAFETY OF A PARACETAMOL + IBUPROFEN COMBINATION IN PATIENTS WITH PRIMARY DYSMENORRHOEA | ||
| Medical condition: DYSMENORRHOEA | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002668-42 | Sponsor Protocol Number: TRA-IV-17-1 | Start Date*: 2017-10-11 |
| Sponsor Name:Laboratoires SMB S.A. | ||
| Full Title: A randomised, interventional, double blind, crossover, controlled study to assess the effect of the administration of paracetamol on tramadol adverse events. | ||
| Medical condition: healthy volunteers (symptomatic treatment of pain) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BG (Completed) | ||
| Trial results: View results | ||
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