- Trials with a EudraCT protocol (14,152)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (284)
14,152 result(s) found for: Intravenous.
Displaying page 1 of 708.
| EudraCT Number: 2011-000022-29 | Sponsor Protocol Number: 013/2011 | Start Date*: 2011-09-21 |
| Sponsor Name:Medizinische Universität Wien | ||
| Full Title: The interaction of intravenous lidocaine on the Cp50 of propofol for skin incision | ||
| Medical condition: the effects of intravenous application of lidocaine on the Cp50 during propofol narcosis should be investigated | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003915-39 | Sponsor Protocol Number: 54811 | Start Date*: 2016-03-07 |
| Sponsor Name: | ||
| Full Title: A Randomized Clinical Trial of Cutaneous Xylocaine Spray to Reduce Intravenous Cannulation Pain in Adults. | ||
| Medical condition: The enrolled subjects will get an intravenous cannulation in both elbows. The subject will get before xylocaine spray is placed, the intervention-arm, one intravenous cannulation in one of the elbo... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019488-12 | Sponsor Protocol Number: Protocol No 1 | Start Date*: 2010-12-08 |
| Sponsor Name:Joint Research Office, Barts and The London NHS Trust | ||
| Full Title: A Single Centre Prospective Randomised Study to Investigate the Metabolism of Intravenous Paracetamol in Humans | ||
| Medical condition: The study is looking at the cerebrospinal fluid pharmacokinetics of intravenous paracetamol. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002046-23 | Sponsor Protocol Number: OY052016 | Start Date*: 2016-08-15 |
| Sponsor Name:Minna Honkila / OYS | ||
| Full Title: Isotonic versus hypotonic intravenous fluids in hospitalised children - a randomised controlled trial | ||
| Medical condition: Acutely ill hospitalised children who need intravenous fluid therapy. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004578-29 | Sponsor Protocol Number: P.sitsen.01 | Start Date*: 2007-06-15 |
| Sponsor Name:Leids Universitair Medisch Centrum | ||
| Full Title: The efficacy of intravenous versus rectal paracetamol: A randomized, prospective, double-blind placebo-controlled study | ||
| Medical condition: Aims of the study 1)to compare the analgesic efficacy of intravenous versus rectal paracetamol versus placebo as assessed by VAS scores and PCA morphine consumption. 2)To assess the pharmacokinet... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-001908-38 | Sponsor Protocol Number: 08042012 | Start Date*: 2012-07-12 |
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie | ||
| Full Title: The effect of intravenous ketamine on the MAC of sevoflurane – a randomized, placebo controlled, double blinded clinical trial | ||
| Medical condition: We want to test if intravenous s-ketamine of two different doses has an effect on MAC of sevoflurane | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-017369-47 | Sponsor Protocol Number: 09/CMC/4659E | Start Date*: 2010-11-30 |
| Sponsor Name:Research and Development Office Cardiff and Vale NHS Trust [...] | ||
| Full Title: An in-vitro observational pilot study of the role of gamma delta T cells in the acute phase reaction to intravenous bisphosphonate; in blood samples donated by patients receiving intravenous bispho... | ||
| Medical condition: Osteoporosis and Paget's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011382-80 | Sponsor Protocol Number: | Start Date*: 2009-06-22 |
| Sponsor Name:Nottingham University Hospital | ||
| Full Title: Intravenous Iron: biomarkers and treatment strategies in anaemic Colorectal cancer patients. | ||
| Medical condition: Anaemia (specifically related to surgical pathology) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000200-14 | Sponsor Protocol Number: | Start Date*: 2005-07-08 |
| Sponsor Name:North Bristol NHS Trust | ||
| Full Title: A randomised, double-blinded comparison of the effectiveness of intravenously administered Ketoralac versus Dexamethasone in the treatment of pain following surgical removal of third molar teeth un... | ||
| Medical condition: Pain experienced after the surgical removal of impacted third molars. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000680-26 | Sponsor Protocol Number: Taurine05 | Start Date*: 2005-06-27 |
| Sponsor Name:North west London Hospital Trust | ||
| Full Title: A randomised double blind controlled crossover trial of intravenous taurine supplementation in parenteral nutrition as an effective treatment for reducing hepatobiliary complications in chronic int... | ||
| Medical condition: Complications of intravenous nutrition include cholestatic liver disease. This is one of the main causes of death during long-term home parenteral nutrition (HPN) and a study in 2000 found that 65%... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-012585-30 | Sponsor Protocol Number: 1 | Start Date*: 2009-08-21 |
| Sponsor Name:NHS Grampian Research and Development | ||
| Full Title: The pharmacokinetics of single and multiple doses of intravenous paracetamol in children | ||
| Medical condition: There is no medical condition to be investigated. This is a pharmacokinetic study to be performed in children routinely treated with intravenous paracetamol for post surgical pain in line with loca... | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012512-41 | Sponsor Protocol Number: 1 | Start Date*: 2009-09-04 |
| Sponsor Name:NHS Grampian | ||
| Full Title: The pharmacokinetics of single and multiple doses of intravenous ketorolac in children | ||
| Medical condition: There is no medical condition being investigated. This is a pharmacokinetic study to be performed in children routinely treated with ketorolac for post surgical pain in line with local treatment pr... | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003332-21 | Sponsor Protocol Number: P160502 | Start Date*: 2017-01-17 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002208-32 | Sponsor Protocol Number: PAR06 | Start Date*: 2006-08-14 |
| Sponsor Name:York Hospital NHS Trust | ||
| Full Title: A comparison of the analgesic efficacy of oral and intravenous paracetamol (perfalgan) in a day case setting | ||
| Medical condition: We will perform a double blind randomised comparison of oral paracetamol versus intravenous paracetamol (Perfalgan) in patients undergoing knee arthroscopy in a day surgery setting. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002386-37 | Sponsor Protocol Number: IVN3ICD | Start Date*: 2007-08-24 |
| Sponsor Name:Department of Cardiology, Aalborg Hospital | ||
| Full Title: Intravenous infusion of n-3 polyunsaturated fatty acids and ventricular tackycardi in patients with implantable cardioverter defibrillator (ICD) | ||
| Medical condition: Patients with an implantable cardioverter defibrillator (ICD-unit) for treatment for cardiac ventricular arrhythmias and for prevention of sudden cardiac death | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002952-17 | Sponsor Protocol Number: COPDIron | Start Date*: 2012-11-12 |
| Sponsor Name:University of Oxford | ||
| Full Title: Effects of intravenous iron on hypoxic pulmonary responses in COPD | ||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-001631-12 | Sponsor Protocol Number: IgPro10_3004 | Start Date*: 2017-01-30 | |||||||||||
| Sponsor Name:CSL Behring KK | |||||||||||||
| Full Title: Prospective open-label single-arm study of the pharmacokinetics and safety of intravenous IgPro10 in Japanese subjects with primary immunodeficiency | |||||||||||||
| Medical condition: Primary immunodeficiency | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024342-30 | Sponsor Protocol Number: CBYM338X2202 | Start Date*: 2011-07-20 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled multi-center study of BYM338 for treatment of cachexia in patients with stage IV non-small cell lung cancer or stage III/IV adenocarcinoma of the panc... | |||||||||||||
| Medical condition: Condition of cachexia in adults with stage IV metastatic non-small cell lung cancer or stage III/IV pancreatic adenocarcinoma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004389-15 | Sponsor Protocol Number: STH14192 | Start Date*: 2007-04-05 |
| Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | ||
| Full Title: The use of Single dose intravenous paracetamol "Perfalgan" in Early extubation cardiac surgery | ||
| Medical condition: Extubation time following coronary artery bypass surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002979-40 | Sponsor Protocol Number: 2006.05 | Start Date*: 2006-08-07 |
| Sponsor Name:LUMC | ||
| Full Title: Pharmacokinetic-pharmacodynamic modeling of S(+)-ketamine in healthy volunteers | ||
| Medical condition: Healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
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