- Trials with a EudraCT protocol (1,494)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (41)
1,494 result(s) found for: Magnetic Resonance Imaging.
Displaying page 1 of 75.
EudraCT Number: 2011-005917-35 | Sponsor Protocol Number: CMC-P014 | Start Date*: 2012-03-20 | |||||||||||
Sponsor Name:CMC Contrast AB | |||||||||||||
Full Title: Accuracy in Diagnosis of Focal Liver Lesions following Oral Administration of CMC-001 Combined with Diffusion Weighted Magnetic Resonance Imaging (MRI) of the Liver. An Open-Label, Non-Randomised, ... | |||||||||||||
Medical condition: Focal Liver Lesions in Diagnosed Cancer Patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005249-13 | Sponsor Protocol Number: Primovist - OATP1B1 | Start Date*: 2007-01-31 | |||||||||||
Sponsor Name:Department of Clinical Pharmacology, University of Greifswald | |||||||||||||
Full Title: Influence of the OATP1B1 genotype on the hepatic uptake of Primovist® in healthy volunteers and in patients with liver disease | |||||||||||||
Medical condition: The trial will be performed in 32 healthy subjects and in 60 patients with a liver disease subjected to MR imaging | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013081-17 | Sponsor Protocol Number: BAY 86-6661/91784 (312046) | Start Date*: 2009-11-20 | |||||||||||
Sponsor Name:Bayer HealthCare Pharmaceuticals, Inc. | |||||||||||||
Full Title: Open-label, multi-center, two-stage, age stratified, pharmacokinetic, safety, and efficacy study in children 2 month to < 2 years of age undergoing Magnevist Injection enhanced MRI | |||||||||||||
Medical condition: Contrast-enhanced MRI in children 2 month to < 2 years | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000867-10 | Sponsor Protocol Number: CD13/10671 | Start Date*: 2014-02-13 | |||||||||||||||||||||
Sponsor Name:University of Leeds | |||||||||||||||||||||||
Full Title: Effects of Aldosterone Antagonism in Heart Failure with Preserved Ejection Fraction (HF-PEF): Cardiac MRI, Echocardiography, Exercise Physiology & Quality of Life Assessment | |||||||||||||||||||||||
Medical condition: Heart failure with a preserved ejection fraction | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001599-12 | Sponsor Protocol Number: ASC-Man-P016 | Start Date*: 2019-10-21 | |||||||||||
Sponsor Name:Ascelia Pharma AB | |||||||||||||
Full Title: A Multicenter, Open-label Study to Evaluate the Safety and Diagnostic Efficacy of Mangoral in Patients with Known or Suspected Focal Liver Lesions and Severe Renal Impairment | |||||||||||||
Medical condition: MRI in terms of visualization of detected focal liver lesions in patients with known or Suspected focal liver lesions and severe renal impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Ongoing) PL (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004153-22 | Sponsor Protocol Number: 310788 | Start Date*: 2007-04-18 | |||||||||||
Sponsor Name:Bayer Schering Pharma AG | |||||||||||||
Full Title: Open-label multi-center study of magnetic resonance imaging (MRI) with 0.1 mmol/kg BW Gadovist (1.0 M) to assess pharmacokinetics, safety and tolerability in children | |||||||||||||
Medical condition: Gadovist as diagnostic imaging agent is approved only for adult patients. Diseases usually representing indications for contrast-enhanced Magnetic Resonance Imaging (CE-MRI) are common also in a pe... | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) DK (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003825-31 | Sponsor Protocol Number: GDX-44-015 | Start Date*: 2022-02-28 | ||||||||||||||||
Sponsor Name:Guerbet | ||||||||||||||||||
Full Title: Gadopiclenol Pharmacokinetics, Safety and Efficacy in Pediatric Patients < 2 Years of Age Undergoing Contrast-enhanced MRI P/0145/2019 | ||||||||||||||||||
Medical condition: Known or highly suspected abnormalities/ lesion(s) as detected by previous imaging examinations (including the fetal imaging) that need to be investigated by contrast-enhanced MRI of any body regio... | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Ongoing) PL (Ongoing) BG (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005886-19 | Sponsor Protocol Number: HGKKRWPHD2 | Start Date*: 2012-07-31 | ||||||||||||||||||||||||||
Sponsor Name:Gastroenterology MIDT | ||||||||||||||||||||||||||||
Full Title: Correlation between intestinal blOod flow assessed by magNetic resonance imaging and ulTRASound Techniques (CONTRAST) | ||||||||||||||||||||||||||||
Medical condition: Crohns Disease with active disease | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000690-78 | Sponsor Protocol Number: 19773 | Start Date*: 2018-10-29 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: LowEr Administered Dose with highEr Relaxivity: Gadovist vs Dotarem | |||||||||||||
Medical condition: Contrast enhancement in magnetic resonance imaging (MRI) for central nervous system (CNS), magnetic resonance (MR) angiography, liver, kidney and other body regions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003089-29 | Sponsor Protocol Number: 69918356615 | Start Date*: 2018-04-06 | ||||||||||||||||||||||||||
Sponsor Name:Medical University of Vienna, Department of Biomedical Imaging and Image-guided Therapy | ||||||||||||||||||||||||||||
Full Title: Measuring hallmarks of cancer for non-invasive characterization of breast lesions by simultaneous multiparametric 18F-ethylcholine PET- MRI – an exploratory study | ||||||||||||||||||||||||||||
Medical condition: Patients with imaging suspected breast cancer (BI-RADS 4&5 on conventional imaging, e.g. mammography and ultrasound). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: AT (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006724-35 | Sponsor Protocol Number: fMRI-CA_2008 | Start Date*: 2008-09-08 | ||||||||||||||||
Sponsor Name:CMIV | ||||||||||||||||||
Full Title: Functional MRI after administration of Gd-based blood pool contrast agents | ||||||||||||||||||
Medical condition: This study aims to investigate the possibility to obtain higher functional contrast and better spatial assessment in contrast enhanced functional Magnetic Resonance Imaging (fMRI) as compared to st... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022772-31 | Sponsor Protocol Number: 20100812v2 | Start Date*: 2011-02-09 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Psychiatrie und Psychotherapie | |||||||||||||
Full Title: Brain Network Dysfunction as a Model for Schizophrenia: Connectivity Alterations using Ketamine and pharmacological Magnetic Resonance Imaging | |||||||||||||
Medical condition: Quantify changes of resting-state functional connectivity in response to Esketamine in healthy volunteers. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002702-63 | Sponsor Protocol Number: 2006RD003 | Start Date*: 2007-03-08 | |||||||||||
Sponsor Name:South Manchester University Hospital NHS Trust | |||||||||||||
Full Title: Does oral Ranitidine improve magnetic resonance cholangio-pancreatogram images allowing clinically useful improvement? | |||||||||||||
Medical condition: Image quality improvement in Magnetic Resonance Cholangio-Pancreatogram scans | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002455-26 | Sponsor Protocol Number: IRON-CMR | Start Date*: 2014-09-20 |
Sponsor Name:Karolinska Institute | ||
Full Title: The use of intravenous Iron oxide as a contrast agent for cardiac magnetic resonance imaging. | ||
Medical condition: Cardiovascular diseases: Acute myocardial infarction, chronic myocardial infarction, myocardial ischemia, myocarditis, diffuse myocardial fibrosis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000952-32 | Sponsor Protocol Number: BAY86-4873/16078 | Start Date*: 2015-09-24 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Open-label, multi-center study to evaluate the safety, efficacy, and plasma gadolinium concentrations after an intravenous injection of 0.1 mL/kg body weight Eovist/Primovist for enhanced magnetic ... | |||||||||||||
Medical condition: Magnetic Resonance Imaging | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005846-36 | Sponsor Protocol Number: HGKKRWPHD | Start Date*: 2012-07-31 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Gastroenterology MIDT | ||||||||||||||||||||||||||||||||||||||
Full Title: Safe evaluation of obstructive crohns disease using bloodflow Time-intensity curves and Elastography correlated to Neutrocytes and collagen counts and biomechanical properties Obtained in Stenotic ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Crohns Disease undergoing elective surgery for intestinal stenosis. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011824-79 | Sponsor Protocol Number: 91686125 | Start Date*: 2009-11-03 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Effects of fluoxetine on the outgrowth of the serotonergic system | |||||||||||||
Medical condition: We investigate whether the effects fluoxetine (Prozac®) on the outgrowth of the serotonergic system are dependent on age. In a 16 week multicenter randomized, double-blind, placebo controlled trial... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003933-33 | Sponsor Protocol Number: 12K3-S-140708 | Start Date*: 2006-12-20 |
Sponsor Name:Bundeswehr | ||
Full Title: Clinical value of Choline-Positron-Emission-Tomography combined with Magnetic Resonance Imaging by software fusion for pre-therapeutic staging of prostate cancer | ||
Medical condition: Clinical value of Choline-Positron-Emission-Tomography combined with Magnetic Resonance Imaging by software fusion for pre-therapeutic staging of prostate cancer referring to histopathological, pos... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002880-33 | Sponsor Protocol Number: PINDEX | Start Date*: 2016-10-28 |
Sponsor Name:University of Turku | ||
Full Title: Bioavailability and pharmacokinetics of intranasal dexmedetomidine in children | ||
Medical condition: Paediatric patients scheduled for minor procedures such as intra-articular drug injections, hernia repair, bronchoscopy or magnetic resonance imaging. | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001836-69 | Sponsor Protocol Number: Vort-MCI_001 | Start Date*: 2021-09-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effects of Vortioxetine in Mild Cognitive Impairment measured by Functional Magnetic Resonance Imaging | ||
Medical condition: Mild cognitive impairment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
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