- Trials with a EudraCT protocol (20)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
		
	   		
	   		    
                    
                   	
                   	    20 result(s) found for: Meglumine.
                    
                
			
   			
		
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| EudraCT Number: 2011-005498-21 | Sponsor Protocol Number: | Start Date*: 2012-07-12 | 
| Sponsor Name:Med. Univ. Wien, Univ. Klinik für Radiodiagnostik | ||
| Full Title: Breast lesion detection and characterization at contrast-Enhanced MRI of the breast: comparison of gadoterate meglumine versus gadobenate dimeglumine at 3 Tesla | ||
| Medical condition: the aim of this study is to intraindividually compare the use of equivalent doses of gadobenate dimeglumine (MultiHance, Bracco Imaging, Milan, Italy) and gadoterate meglumine (DOTAREM, Guerbet, Fr... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-000868-42 | Sponsor Protocol Number: B3461045 | Start Date*: 2016-09-26 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: A PHASE 3 MULTICENTER, RANDOMIZED, DOUBLE-BLIND, EXTENSION STUDY TO EVALUATE THE SAFETY OF DAILY ORAL DOSING OF TAFAMIDIS MEGLUMINE (PF-06291826) 20 MG OR 80 MG IN SUBJECTS DIAGNOSED WITH TRANSTHYR... | |||||||||||||
| Medical condition: Transthyretin amyloid cardiomyopathy (TTR-CM) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) BE (Completed) CZ (Completed) DE (Completed) SE (Completed) NL (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003026-14 | Sponsor Protocol Number: ML-3341-306 | Start Date*: 2016-02-04 | |||||||||||
| Sponsor Name:Melinta Therapeutics, Inc. | |||||||||||||
| Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, COMPARATOR-CONTROLLED STUDY TO EVALUATE THE SAFETY AND EFFICACY OF INTRAVENOUS TO ORAL DELAFLOXACIN IN ADULT SUBJECTS WITH COMMUNITY-ACQUIRED BACTE... | |||||||||||||
| Medical condition: Community-Acquired Bacterial Pneumonia | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Completed) LV (Completed) BG (Completed) DE (Completed) SI (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-002465-35 | Sponsor Protocol Number: B3461028 | Start Date*: 2014-04-07 | |||||||||||
| Sponsor Name:FoldRx Pharmaceuticals, a Pfizer Company | |||||||||||||
| Full Title: A multicentre, international, phase 3, double-blind, placebo-controlled, randomized study to evaluate the efficacy, safety and tolerability of daily oral dosing of tafamidis meglumine (PF-06291826)... | |||||||||||||
| Medical condition: Transthyretin amyloid cardiomyopathy (TTR-CM) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) IT (Completed) ES (Completed) DE (Completed) SE (Completed) CZ (Completed) NL (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-009426-81 | Sponsor Protocol Number: CIA-GaDo | Start Date*: 2009-11-10 | |||||||||||
| Sponsor Name:University Heidelberg | |||||||||||||
| Full Title: Contrast-enhanced Imaging of the Abdomen: Gadovist® vs. Dotarem® – Intraindividual comparison of 0.1mmol/kg bw gadoterate meglumine with 0.1mmol/kg bw gadobutrol for dynamic abdominal imaging in pa... | |||||||||||||
| Medical condition: patients with suspected focal liver or renal lesions | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021526-36 | Sponsor Protocol Number: LMU_Rad_MR_GadoMRA01 | Start Date*: 2011-04-07 | |||||||||||
| Sponsor Name:Klinikum der Universität München | |||||||||||||
| Full Title: Dynamic and high-resolution MR angiography of the supraaortic vessels at 3 Tesla: Performance of Gadobutrol (Gadovist) in comparison to Gedobenate Dimeglumine (Multihance) and Gadoterate Meglumine ... | |||||||||||||
| Medical condition: Supraaortic vessel disease; suspicion or proven carotid artery stenosis / stenoses | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024096-87 | Sponsor Protocol Number: Ileus_gastro | Start Date*: 2011-07-01 | |||||||||||
| Sponsor Name:Sebastiano Biondo Aglio | |||||||||||||
| Full Title: ESTUDIO CLÍNICO PROSPECTIVO ALEATORIZADO DOBLE CIEGO SOBRE LA UTILIDAD TERAPÉUTICA DEL GASTROGRAFÍN EN ÍLEO PARALÍTICO EN EL POSTOPERATORIO DE CIRUGÍA COLORRECTAL | |||||||||||||
| Medical condition: Ileo paralítico postoperatorio | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001300-30 | Sponsor Protocol Number: 2017_CERVPLEX_1.1 | Start Date*: 2017-10-03 | 
| Sponsor Name:UK für Anästhesieologie, Gemeinn. Sbg. Landeskliniken BetriebsgesmbH | ||
| Full Title: Comparison of deep, intermediate and superficial cervical plexus block for carotid endarterectomies concerning paresis of the phrenic nerve, lung function and tissue distribution: a prospective, ra... | ||
| Medical condition: deep, intermediate or superficial cervical plexus block for carotid endarterectomy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-013432-20 | Sponsor Protocol Number: ISI2009-02 | Start Date*: 2009-08-04 | |||||||||||
| Sponsor Name:Charité Campus Mitte | |||||||||||||
| Full Title: Intra-individual, randomized comparison of the MRI contrast agents gadobutrol versus gadoterate meglumine in breast MR imaging | |||||||||||||
| Medical condition: Breast tumor | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011535-12 | Sponsor Protocol Number: Fx1A-303 | Start Date*: 2009-08-26 | |||||||||||
| Sponsor Name:Pfizer Inc. | |||||||||||||
| Full Title: Open-Label Safety and Efficacy Evaluation of Fx-1006A in Patients with Transthyretin Amyloidosis | |||||||||||||
| Medical condition: Transthyretin Amyloidosis (ATTR) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) FR (Completed) PT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002409-75 | Sponsor Protocol Number: Dota-PrimoLIV | Start Date*: 2014-01-06 | ||||||||||||||||
| Sponsor Name:Charite | ||||||||||||||||||
| Full Title: Intra-individual, comparison of the MRI contrast agents gadoxetic acid (Primovist®) versus gadoterate meglumine (Dotarem®) in liver MRI of patients with HCC and underlying cirrhosis | ||||||||||||||||||
| Medical condition: Patients with liver cirrhosis and diagnosis of hepatocellular carcinoma based on noninvasive HCC diagnostic (EASL) criteria | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-004983-39 | Sponsor Protocol Number: RX-3341-303 | Start Date*: 2015-01-26 | |||||||||||
| Sponsor Name:Melinta Therapeutics, Inc | |||||||||||||
| Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF IV AND ORAL DELAFLOXACIN COMPARED WITH VANCOMYCIN + AZTREONAM IN PATIENTS WITH ACUTE... | |||||||||||||
| Medical condition: ACUTE BACTERIAL SKIN AND SKIN STRUCTURE INFECTIONS | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) EE (Completed) LV (Completed) SK (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004730-42 | Sponsor Protocol Number: IQVIA-ODYS-001-LZA45541 | Start Date*: 2022-10-24 | |||||||||||||||||||||||||||||||
| Sponsor Name:IQVIA RDS FRANCE SAS | |||||||||||||||||||||||||||||||||
| Full Title: Prospective evaluation of potential effects of repeated gadolinium-based contrast agent (GBCA) administrations of the same GBCA on motor and cognitive functions in neurologically normal adults in c... | |||||||||||||||||||||||||||||||||
| Medical condition: Long term potential effect of repeated exposure to either a linear or a macrocyclic gadolinium-based contrast agent (GBCA) on change from baseline to Year 5 in motor and cognitive function among ne... | |||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: NL (Completed) IT (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2014-000473-39 | Sponsor Protocol Number: CIR-ILI-2014 | Start Date*: 2015-01-19 | |||||||||||
| Sponsor Name:Fundacio Parc Taulí | |||||||||||||
| Full Title: Randomized and prospective clinical trial about the therapeutic use of diatrizoic acid (Gastrografin®) in postoperative ileus. | |||||||||||||
| Medical condition: Postoperative paralytic Ileus | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005693-31 | Sponsor Protocol Number: 312021 | Start Date*: 2008-03-04 | |||||||||||
| Sponsor Name:BAYER | |||||||||||||
| Full Title: Contrast-enhanced MRI examination of cerebral neoplastic enhancing lesions: comparison of diagnostic efficacy of Gd-DOTA 0.5 M and gadobutrol 1.0 M at 0.1 mmol Gd/kg body weight: Intra-individual ... | |||||||||||||
| Medical condition: patients with cerebral neoplastic lesions | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001582-33 | Sponsor Protocol Number: Er-01-Perf-Stroke | Start Date*: 2012-09-19 | 
| Sponsor Name:University Hospital Erlangen | ||
| Full Title: Intraindividual cross-over comparison of Gadobutrol and Gadoterate enhanced combined DSC-MR-Perfusion and MR-Angiography in patients with cerebrovascular disease | ||
| Medical condition: Patients with high grade carotid artery stenosis or acute cerebral ischemia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-001767-71 | Sponsor Protocol Number: RX-3341-302 | Start Date*: 2013-06-20 | |||||||||||
| Sponsor Name:Melinta Therapeutics, Inc | |||||||||||||
| Full Title: A PHASE 3, MULTICENTER, RANDOMIZED, DOUBLE BLIND, ACTIVE CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF DELAFLOXACIN COMPARED WITH VANCOMYCIN + AZTREONAM IN PATIENTS WITH ACUTE BACTERIAL S... | |||||||||||||
| Medical condition: ACUTE BACTERIAL SKIN AND SKIN STRUCTURE INFECTIONS | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) LV (Completed) ES (Completed) BG (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014691-21 | Sponsor Protocol Number: GAND-emesis | Start Date*: 2010-01-27 | |||||||||||||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||||||||||||
| Full Title: GAND-emesis: A multinational, randomized, double-blind, placebo-controlled, parallel-group study to investigate the efficacy and tolerability of palonosetron and dexamethasone plus the neurokinin1... | |||||||||||||||||||||||
| Medical condition: The study aims at investigating if a three-drug antiemetic regimen is superior in preventing nausea and vomiting in patients receiving radiotherapy and weekly chemotherapy than a two-drug regimen (... | |||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2009-012607-26 | Sponsor Protocol Number: MIMEB | Start Date*: 2009-12-10 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:University of Cologne | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: MIMEB - Molecular Imaging with erlotinib and bevacizumab. A Phase II Clinical Trial to Evaluate the Accuracy of FDG-/FLT-PET and DCE-MRI for Early Prediction of Non-Progression in Patients with Adv... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients with Advanced Non Squamous Cell Non Small Cell Lung Cancer (NSCLC), first-line. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2010-020319-34 | Sponsor Protocol Number: DGD 44-050 | Start Date*: 2010-09-30 | |||||||||||
| Sponsor Name:GUERBET | |||||||||||||
| Full Title: SAFETY AND EFFICACY EVALUATION OF DOTAREM® IN MAGNETIC RESONANCE IMAGING (MRI) IN PATIENTS WITH CENTRAL NERVOUS SYSTEM (CNS) LESIONS | |||||||||||||
| Medical condition: Patient with Central Nervous System (CNS) Lesions | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) ES (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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