- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
21 result(s) found for: Contrast-induced nephropathy.
Displaying page 1 of 2.
EudraCT Number: 2009-013547-11 | Sponsor Protocol Number: 09-059 | Start Date*: 2009-07-16 | |||||||||||
Sponsor Name:Leids Universitair Medisch Centrum | |||||||||||||
Full Title: Sodium Bicarbonate for the prevention of Contrast Induced Nephropathy in patients undergoing CTPA | |||||||||||||
Medical condition: The prevention of Contrast Induced Nephropathy is under investigation. Contrast induced nephropathy (CIN) can occur after injecting radiographic iso osmolair contrast media. Patients with a renal i... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002032-33 | Sponsor Protocol Number: NICIR | Start Date*: 2016-07-20 | |||||||||||
Sponsor Name:Fundacio Privada Clinic per a la Recerca Biomedica | |||||||||||||
Full Title: Comparative study of the efficacy of oral versus intravenous hydration as a preventive measure of contrast-induced nephropathy (CIN) in patients with renal insufficiency (RI) grade III under study ... | |||||||||||||
Medical condition: Patients with renal failure undergoing a computed tomography scan with contrast | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003696-18 | Sponsor Protocol Number: uni-koeln-1547 | Start Date*: 2013-07-25 |
Sponsor Name:University of Cologne | ||
Full Title: Effect of a preinterventional calorie restriction on renal function after contrast agent exposition in patients at risk. | ||
Medical condition: contrast-induced nephropathy, acute renal failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001838-29 | Sponsor Protocol Number: TEATE | Start Date*: 2015-01-08 | ||||||||||||||||
Sponsor Name:"G. d'Annunzio" University | ||||||||||||||||||
Full Title: PrevenTion of contrast‐inducEd nephroAThy with urinE alkalinization: the TEATE study | ||||||||||||||||||
Medical condition: contrast‐induced nephroathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001986-32 | Sponsor Protocol Number: 2005RA02 | Start Date*: 2005-07-29 |
Sponsor Name:NHS Tayside | ||
Full Title: Comparison of 2 contrast agents in preventing acute renal failure after angiography | ||
Medical condition: Peripheral vascular or renovascular disease being investigated by angiography | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-001229-15 | Sponsor Protocol Number: PNIC-Na | Start Date*: 2013-08-14 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario Ramón y Cajal | ||
Full Title: The efficacy of oral and intravenous administration of sodium chloride in the prophylaxis of nephropathy induced by iodinated contrasts in outpatients | ||
Medical condition: Patients at high risk of developing an iodinated contrast-induced nephropathy. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011175-70 | Sponsor Protocol Number: 805 | Start Date*: 2009-05-28 | |||||||||||||||||||||
Sponsor Name:Liverpool Heart and Chest Hospital | |||||||||||||||||||||||
Full Title: A randomised factorial trial of N-acetylcysteine prophylaxis and iso-osmolar versus low-osmolar contrast media on kidney function in patients at risk of contrast induced nephropathy following cardi... | |||||||||||||||||||||||
Medical condition: Contrast-induced nephropathy following cardiac catheterisation | |||||||||||||||||||||||
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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: 2011-003611-37 | Sponsor Protocol Number: PREVENT-CINHF | Start Date*: 2011-10-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA' DI NOVARA | |||||||||||||
Full Title: PRevEntion of cardiac and Vascular pEriprocedural complications in patients undergoiNg coronary angiography or angioplasTy: hydratation vs carbonates to prevent Contrast-Induced Nephropathy in pati... | |||||||||||||
Medical condition: Patients undergoing coronary angiography or angioplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008491-13 | Sponsor Protocol Number: 2008-008491-13 | Start Date*: 2009-03-07 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA USL 8 AREZZO | ||||||||||||||||||||||||||||
Full Title: A Multicentric randomized comparison between iso-osmolar and ipo-osmolar contrast agents in STEMI patients undergoing primary PCI. Assessment of contrast-induced nephropathy incidence and myocardia... | ||||||||||||||||||||||||||||
Medical condition: Patients with Acute Myocardial Infarction within 12 hours after the onset of symptoms | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000087-12 | Sponsor Protocol Number: DXV406 | Start Date*: 2005-08-16 | |||||||||||
Sponsor Name:Amersham Health S.A. (parte de GE Healthcare Ltd y sus filiales) | |||||||||||||
Full Title: Estudio multicéntrico, aleatorizado, doble ciego, de grupos paralelos, en fase IV, para comparar los efectos renales del medio de contraste no iónico isosmolar, iodixanol 320 mg I/ml (VisipaqueTM),... | |||||||||||||
Medical condition: Subjects with a combination of diabetes mellitus (type I or II), and impaired renal function. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007546-36 | Sponsor Protocol Number: NaHCO3 | Start Date*: 2008-03-20 | ||||||||||||||||
Sponsor Name:Institute for Clinical and Experimental Medicine | ||||||||||||||||||
Full Title: Sodium Bicarbonate for Prevention of Contrast-Induced Nephropathy in Diabetic Patients with Renal Insufficiency | ||||||||||||||||||
Medical condition: Diabetes mellitus with renal insufficiency | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000712-42 | Sponsor Protocol Number: IOM-115 | Start Date*: 2004-12-22 |
Sponsor Name:Bracco Imaging S.p.A. | ||
Full Title: Enhacement of the lower extremities computed tomography: IOMERON®-400 VS VISIPAQUE™-320 (ELECTIV). | ||
Medical condition: subjects with mild to moderate renal impairment (SCr =1.5-2.5 mg/dL and/or calculated CrCl = 10-60 mL/min) who undergo clinically-indicated IV contrast-enhanced MDCTA scanning of the lower extremit... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) SE (Completed) GB (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-000711-26 | Sponsor Protocol Number: IOM-114 | Start Date*: 2004-12-22 |
Sponsor Name:Bracco Imaging S.p.A. | ||
Full Title: ABDOMINAL COMPUTED TOMOGRAPHY: IOMERON®400 VS VISIPAQUE™320 ENHANCEMENT (ACTIVE). | ||
Medical condition: subjects with mild to moderate renal impairment scheduled to undergo clinically-indicated IV contrast –enhanced MDCT scanning of the liver | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) SE (Prematurely Ended) GB (Prematurely Ended) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-019740-39 | Sponsor Protocol Number: COMEDIANS | Start Date*: 2010-04-26 | |||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
Full Title: Isotonic contrast (iodixanol) administration vs. low osmolar contrast (iopromide) use: evaluating risk of contrast-induced nephropathy in cancer patients at very low risk | |||||||||||||
Medical condition: Oncological patients undergoing to diagnostic imaging | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001668-13 | Sponsor Protocol Number: GE-012-106 | Start Date*: 2017-10-25 | ||||||||||||||||
Sponsor Name:GE Healthcare Ltd. and its Affiliates | ||||||||||||||||||
Full Title: Parallel-Group, Placebo-Controlled Randomized Study Investigating the Effect of Intravenous Iso-osmolar Iodinated Contrast Material Iodixanol (Visipaque™ Injection 320 mgI/mL) on Renal Function in ... | ||||||||||||||||||
Medical condition: Chronic Kidney Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) GB (Prematurely Ended) BE (Prematurely Ended) HU (Completed) PL (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000229-23 | Sponsor Protocol Number: DGD 44-044 | Start Date*: 2007-08-24 | |||||||||||
Sponsor Name:GUERBET | |||||||||||||
Full Title: RENAL SAFETY EVALUATION AFTER DOTAREM-ENHANCED MRA COMPARED WITH NON-ENHANCED MRI IN PATIENTS AT HIGH RISK OF DEVELOPING CONTRAST MEDIUM INDUCED NEPHROPATHY. | |||||||||||||
Medical condition: Patients suffering from renal insufficiency and scheduled for contrast enhanced-MR angiography or unenhanced-MRI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005140-16 | Sponsor Protocol Number: KAI-9803-004 | Start Date*: 2009-06-02 | |||||||||||
Sponsor Name:KAI Pharmaceuticals, Inc | |||||||||||||
Full Title: Inhibition of δ-PROTEin kinase C for the reducTION of infarct size in Acute Myocardial Infarction (PROTECTION AMI) | |||||||||||||
Medical condition: Acute Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) ES (Completed) HU (Completed) CZ (Completed) PT (Completed) BE (Completed) SE (Completed) FI (Completed) IT (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001200-23 | Sponsor Protocol Number: CCFM 103/208 | Start Date*: 2008-07-13 | |||||||||||
Sponsor Name:FONDAZIONE MONZINO CENTRO CARDIOLOGICO | |||||||||||||
Full Title: A Study to Evaluate the Effectiveness of Induced Diuresis with Matched Hydration Therapy Compared to Standard Overnight Hydration in the Prevention of Contrast Induced Nephropathy | |||||||||||||
Medical condition: Patients with moderate to severe renal failure candidates to angiographic procedures at high risk for CIN | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002824-42 | Sponsor Protocol Number: SPIRI-201 | Start Date*: 2012-04-17 | |||||||||||
Sponsor Name:Stealth Peptides Inc. | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety, Tolerability and Efficacy of Intravenous Bendavia™ (MTP-131) on Reperfusion Injury in Patients Treated with St... | |||||||||||||
Medical condition: Reperfusion injury in ST-segment Elevation Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019013-13 | Sponsor Protocol Number: IOP-116 | Start Date*: 2010-10-28 | ||||||||||||||||
Sponsor Name:BRACCO IMAGING | ||||||||||||||||||
Full Title: A Phase IV Pilot Study to Evaluate Kidney Damage Measured by Neutrophil Gelatinase- Associated Lipocalin (NGAL) as a New Bio-Marker in Patients with Normal eGFR Undergoing Percutaneous Coronary I... | ||||||||||||||||||
Medical condition: patients that are scheduled to undergo PCI with normal kidney function. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
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