- Trials with a EudraCT protocol (485)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (25)
485 result(s) found for: Morphine.
Displaying page 1 of 25.
EudraCT Number: 2005-002308-40 | Sponsor Protocol Number: IN Morphine II | Start Date*: 2005-08-19 |
Sponsor Name:University of Plymouth | ||
Full Title: Evaluation of Intranasal (IN) Morphine Sulphate as a Paramedic Administered Analgesic for Children in the Pre-Hospital Environment | ||
Medical condition: This research hopes to bridge the gap between in-hospital diamorphine and pre-hospital IV morphine by developing IN morphine for administration to children between 3 and 14 years old. This will all... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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: 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: 2016-001143-40 | Sponsor Protocol Number: OBEMO1EXT | Start Date*: 2016-06-22 |
Sponsor Name:Therapeutic Research Unit | ||
Full Title: Long-term effects of Roux-en-Y Gastric Bypass on morphine exposure after oral administration of immediate release morphine, in comparison with subjects without surgery | ||
Medical condition: Subjects volunteers who undergone Roux-en-Y gastric bypass (RYGB) for at least 48 months and control subjects matched for BMI, age and sex | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002623-29 | Sponsor Protocol Number: Lundbeckstudy2016 | Start Date*: 2016-08-29 |
Sponsor Name:Aalborg Universitets Hospital | ||
Full Title: The Effect of Morphine on the Human Central Nervous System | ||
Medical condition: Healthy volunteers (Brain response to i.v. morphine) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006579-19 | Sponsor Protocol Number: MP-EG-002 | Start Date*: 2007-04-19 | |||||||||||
Sponsor Name:Egalet a/s | |||||||||||||
Full Title: A double-blind, randomized, 2-way cross-over, phase II, efficacy trial in cancer patients to assess the overall efficacy, patient preference, morphine related side effect profile and safety of the ... | |||||||||||||
Medical condition: cancer patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005903-34 | Sponsor Protocol Number: KKSMUW2011-09 | Start Date*: 2012-05-04 |
Sponsor Name:G. L. Pharma GmbH | ||
Full Title: Phase II, single centre, double blinded, cross-over dose confirmation study using two morphine-naloxone i.v. solutions | ||
Medical condition: Treatment of opioid dependence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005619-24 | Sponsor Protocol Number: NL-MAIV-10-2007 | Start Date*: 2007-12-06 |
Sponsor Name:ErasmusmMC/ Sophia Children Hospital | ||
Full Title: Morphine intravenous vs. Acetaminophen intravenous in neonates and young infants undergoing major non-cardiac surgery. | ||
Medical condition: Patients after non-cardiac thoracic or abdominal major surgery receive Morphine as pain relief medication whereas this is associated with Morphine related side effects. In these patients a non-opio... | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003722-18 | Sponsor Protocol Number: 24862486 | Start Date*: 2007-12-10 |
Sponsor Name:St. Antonius Ziekenhuis | ||
Full Title: Randomized clinical trial of the optimization of procedural pain control in Intensive Care patients | ||
Medical condition: all patients admitted to the ICU of the St. Antonius hospital (>18 years old) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003571-19 | Sponsor Protocol Number: RBH2019/001 | Start Date*: 2020-05-21 | |||||||||||
Sponsor Name:Royal Brompton and Harefield NHS Foundation Trust | |||||||||||||
Full Title: PAciFy Cough: A multicentre, double blind, placebo controlled, crossover trial of morphine sulfate for the treatment of PulmonAry Fibrosis Cough | |||||||||||||
Medical condition: Idiopathic pulmonary fibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004380-37 | Sponsor Protocol Number: 0 | Start Date*: 2016-05-03 |
Sponsor Name:University Hospital Sjaelland, Roskilde,Palliative Unit | ||
Full Title: Oral morphine drops for rapid treatment of dyspnea in palliative cancer patients | ||
Medical condition: Morphine drops for palliation of breathlessness in palliative cancer patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003427-14 | Sponsor Protocol Number: AHUS_PAL_21_01 | Start Date*: 2021-12-20 |
Sponsor Name:Akershus University Hospital | ||
Full Title: A randomized controlled trial of subcutaneous versus intravenous morphine when switching from oral to parenteral route in palliative cancer patients | ||
Medical condition: Cancer pain not responding to oral opioids in palliative cancer patient, where switching to the parenteral route is indicated. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001783-21 | Sponsor Protocol Number: 3288 | Start Date*: 2012-07-11 | |||||||||||
Sponsor Name:Childrens's Research Institute | |||||||||||||
Full Title: Optimizing Pain Treatment in Pre-Term Neonates | |||||||||||||
Medical condition: Critically Ill Premature Neonates between 23 and 32 weeks of gestation who are receiving morphine as part of their routine medical management of pain or other medically indicated condition for whic... | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004620-12 | Sponsor Protocol Number: dyspnoea1 | Start Date*: 2005-01-14 |
Sponsor Name:Royal Marsden Hospital | ||
Full Title: Assessment of normal release morphine in the management of dyspnoea | ||
Medical condition: Breathlessness of any cause in cancer patients are identified and treated with normal release morphine which has been shown to be both effective and safe.The idea of the trial is to see if there wi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006846-24 | Sponsor Protocol Number: HTA074801 | Start Date*: 2009-02-27 |
Sponsor Name:North West London Hospitals NHS Trust | ||
Full Title: An Evaluation of the Effectiveness of Ibuprofen and Morphine for Acute Pain in Sickle Cell Disease | ||
Medical condition: Sickle Cell Disease | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001814-34 | Sponsor Protocol Number: OPI 04/006 | Start Date*: 2006-09-12 |
Sponsor Name:The Norwegian University of Science and Technology | ||
Full Title: Effects of hypothermia on the disposition of morphine, fentanyl, midazolam and propofol in intensive care unit patients | ||
Medical condition: Patients treated with therapeutic hypothermia (33-34 °C) and a control group of normothermic patients matched on sex, age and duration of morphine infusion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023844-34 | Sponsor Protocol Number: ParCS | Start Date*: 2011-06-30 | |||||||||||
Sponsor Name:Sint Maartenskliniek | |||||||||||||
Full Title: Effectiveness and safety of parecoxib in children undergoing scoliosis surgery compared to placebo: a double-blinded randomised controlled trial | |||||||||||||
Medical condition: Postoperative pain in children after scoliosis surgergy (spinal fusion). The morphine consumption on the first two postoperative days will be assessed. Children: <18 years old, ASA I or II | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002239-97 | Sponsor Protocol Number: P060402 | Start Date*: 2007-11-22 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Ketamine en association avec une PCA morphine dans le traitement analgésique postopératoire de patients opérés de prothèse totale de hanche (PTH) | |||||||||||||
Medical condition: Patients opérés d'une prothèse totale de hanche | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001410-20 | Sponsor Protocol Number: NL81154.091.22 | Start Date*: 2022-09-21 |
Sponsor Name:Radboud university medical center | ||
Full Title: Determining the clinical relevance of the interaction between enzalutamide and the opioid morphine and the DOAC edoxaban to improve rational pharmacological care of patients with prostate cancer | ||
Medical condition: Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002625-20 | Sponsor Protocol Number: SC052021 | Start Date*: 2021-08-31 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Intrathecal morphine administration for minimally invasive pancreatic surgery: A double blind, prospective randomized placebo-controlled trial. | ||
Medical condition: postoperative pain treatment after minimally invasive pancreatic surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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