- Trials with a EudraCT protocol (191)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
191 result(s) found for: Intravenous Morphine.
Displaying page 1 of 10.
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: 2011-005903-34 | 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: 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: 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: 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: 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: 2008-008527-14 | Sponsor Protocol Number: Q8012-001 | Start Date*: 2009-06-02 | ||||||||||||||||
Sponsor Name:University of Witten/Herdecke | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Active Controlled Study Comparing the Intravenous Dose of Morphine and Oxycodone Combined in a Ratio of 1:1 Versus Morphine Alone Required to Achieve Effective Pain Cont... | ||||||||||||||||||
Medical condition: To determine whether the intravenous coadministration of morphine and oxycodone has fewer opioid related adverse effects (AEs) than morphine alone at doses that result in effective and equi-analges... | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (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: 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 |
EudraCT Number: 2013-001665-16 | Sponsor Protocol Number: 1312 | Start Date*: 2013-08-01 |
Sponsor Name:University Hospital Grenoble | ||
Full Title: Intranasal Sufentanyl analgesia Versus Morphine IV in Emergency room. | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004038-28 | Sponsor Protocol Number: Zalviso | Start Date*: 2018-02-21 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Comparative Prospective Randomized Study in Postoperative Cardiac Surgery Patients on Analgesia with Morphine Continuous Infusion or Sublingual Sufentanil (Zalviso®). | ||
Medical condition: -Postoperative pain treatment after cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004088-19 | Sponsor Protocol Number: TCI-PCA-002 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Postoperative pain treatment after elective cardiac surgery using patient-controlled target-controlled infusion (TCI-PCA) with hydromorphone vs. patient-controlled analgesia (PCA) with morphine | |||||||||||||
Medical condition: Postoperative pain treatment after elective cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002024-41 | Sponsor Protocol Number: P051048 | Start Date*: 2007-02-12 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Etude de l'efficacité de la kétamine à faibles doses analgésiques, en association avec les morphiniques, dans le traitement de la douleur cancéreuse rebelle | |||||||||||||
Medical condition: Analgésie , traitement de la douleur cancéreuse rebelle | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001499-73 | Sponsor Protocol Number: GDW04/2014Amendment1 | Start Date*: 2014-07-31 | |||||||||||
Sponsor Name:University Hospitals Leuven | |||||||||||||
Full Title: Transversus abdominis plane blok, continous systemic administration of lidocain and patient controlled intravenous morphine - 3 methods for postoperative pain control after laparoscopic colorectal ... | |||||||||||||
Medical condition: postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001835-20 | Sponsor Protocol Number: OZBS12.15060 | Start Date*: 2016-01-20 |
Sponsor Name:Erasmus MC | ||
Full Title: Morphine intravenous vs. paracetamol intravenous after cardiac surgery in neonates and infants. | ||
Medical condition: congenital cardiac defects | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002824-19 | Sponsor Protocol Number: NA | Start Date*: 2021-08-12 |
Sponsor Name:CHU de Liège | ||
Full Title: Study of the hypnotic and anti-nociceptive components of Magnesium using Electroencephalogram Spectral Entropy and pupillometry during total intravenous general anesthesia : a randomized double-bli... | ||
Medical condition: Total thyroidectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003795-37 | Sponsor Protocol Number: CCR2644 | Start Date*: 2005-10-31 |
Sponsor Name:The Royal Marsden NHS Foundation Trust | ||
Full Title: Response to Parenteral Morphine and Oxycodone in Acute Pain. | ||
Medical condition: Post operative pain control in patients who have undergone major breast surgery for underlying breast cancer. Major breast surgery constitutes; • Mastectomy • Axillary clearance +/- wide local ex... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
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