- Trials with a EudraCT protocol (1,317)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    1,317 result(s) found for: Renal capsule.
                    
                
			
   			
		
		Displaying page 1 of 66.
	
	
	| EudraCT Number: 2007-006606-16 | Sponsor Protocol Number: F003MN0307_1 | Start Date*: 2008-07-11 | |||||||||||
| Sponsor Name:University of Wuerzburg | |||||||||||||
| Full Title: The Effects of Paricalcitol capsules on Inflammation (CRP levels) and Calcification regulation (fetuin-A levels) in CKD stage 5D patients | |||||||||||||
| Medical condition: Chronic kidney disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003081-32 | Sponsor Protocol Number: 1160.166 | Start Date*: 2012-04-18 | ||||||||||||||||
| Sponsor Name:Boehringer Ingelheim bv | ||||||||||||||||||
| Full Title: An exploratory study to investigate the pharmacokinetics and effects of DABIgatran etexilate in patients with stable severe RENAL disease: DabiRenal | ||||||||||||||||||
| Medical condition: Chronic kidney disease and coagulation | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-002744-24 | Sponsor Protocol Number: 1058/12 | Start Date*: 2012-12-16 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Effect of oral paricalcitol on endothelial function and FGF-23 in peritoneal dialysis patients: a pilot study | |||||||||||||
| Medical condition: CHRONIC RENAL FAILURE | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-006168-30 | Sponsor Protocol Number: RLH_Pentoxifylline_Dec2011 | Start Date*: 2013-01-08 | |||||||||||
| Sponsor Name:R&D, Barts and The London NHS Trust | |||||||||||||
| Full Title: PEntoxifylline in Anaemia Resistant to erythropoietin (PEAR) | |||||||||||||
| Medical condition: We shall study patients with renal failure on dialysis. We shall particularly focus on patients with evidence of erythopoeitin stimulating agent (ESA) resistance. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016159-23 | Sponsor Protocol Number: ViRTUE-2009 | Start Date*: 2011-10-18 | |||||||||||
| Sponsor Name:University Medical Center Groningen (UMCG) | |||||||||||||
| Full Title: Vitamin D in addition to RAAS blockade and dietary sodium for the Treatment of Urinary Excretion of albumin: the ViRTUE-study | |||||||||||||
| Medical condition: chronic kidney disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-005003-88 | Sponsor Protocol Number: SIM15 | Start Date*: 2016-03-15 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
| Full Title: Survival Improvement with Cholecalciferol in Patients on Dialysis – The SIMPLIFIED Registry Trial | |||||||||||||
| Medical condition: Kidney Failure (requiring dialysis). | |||||||||||||
					
						
							
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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: 2009-017619-14 | Sponsor Protocol Number: EBP_TL_2009 | Start Date*: 2010-03-26 | |||||||||||
| Sponsor Name:Medicinsk Forskningsafsnit, Holstebro | |||||||||||||
| Full Title: RENO- OG KREDSLØBSPROTEKTIV EFFEKT AF VITAMIN-D-ANALOG (PARICALCITOL) HOS PATIENTER MED MODERAT TIL SVÆR KRONISK NYREINSUFFICIENS | |||||||||||||
| Medical condition: The aim is to measure the effect of paricalcitol given orally in patients with moderate to severe chronic kidney diseases (CKD stage III-IV i.e. eGFR:15-59 ml/min) investigating vasoactive hormones... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001033-12 | Sponsor Protocol Number: 12020 | Start Date*: 2020-10-13 | |||||||||||
| Sponsor Name:Niels Eske Bruun | |||||||||||||
| Full Title: PROPHYLACTIC ANTIBIOTIC TREATMENT IN END-STAGE KIDNEY DISEASE AND CENTRAL VENOUS CATHETER AS HEMODIALYSIS VASCULAR ACCESS | |||||||||||||
| Medical condition: Severe infection in patients end stage kidney disease and in hemodialysis with CVC as vascular asscess. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000304-41 | Sponsor Protocol Number: FG-506E-12-03 | Start Date*: 2004-12-15 | |||||||||||
| Sponsor Name:Astellas Pharma GmbH | |||||||||||||
| Full Title: A MULTICENTRE, 1:1 RANDOMISED, DOUBLE BLIND, TWO ARM PARALLEL GROUP STUDY TO EVALUATE AND COMPARE THE EFFICACY AND SAFETY OF MODIFIED RELEASE TACROLIMUS FK506E (MR4) VERSUS TACROLIMUS FK506 IN COMB... | |||||||||||||
| Medical condition: Patients with end stage kidney disease who will undergo renal transplantation | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SE (Completed) HU (Completed) FI (Completed) AT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000520-32 | Sponsor Protocol Number: FG-506-02-42 | Start Date*: 2005-01-26 | |||||||||||
| Sponsor Name:Fujisawa GmbH | |||||||||||||
| Full Title: A MULTICENTRE, RANDOMISED, OPEN CLINICAL STUDY TO COMPARE THE EFFICACY AND SAFETY OF A COMBINATION OF TACROLIMUS AND MYCOPHENOLATE MOFETIL BASED REGIMEN WITH OR WITHOUT INDUCTION IN ELDERLY RECIPIE... | |||||||||||||
| Medical condition: Patients with end stage kidney disease who will undergo primary renal transplantion or retransplantation | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004101-32 | Sponsor Protocol Number: D4325C00001 | Start Date*: 2021-04-06 | |||||||||||
| Sponsor Name:AstraZeneca | |||||||||||||
| Full Title: A Phase 2b Multicentre, Randomised, Double-Blind, Placebo-Controlled, Parallel Group Dose-Ranging Study to Assess the Efficacy, Safety and Tolerability of Zibotentan and Dapagliflozin in Patients w... | |||||||||||||
| Medical condition: Chronic Kidney Disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) NL (Completed) BG (Completed) DK (Completed) IT (Completed) ES (Restarted) SK (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001824-36 | Sponsor Protocol Number: 201201 | Start Date*: 2012-07-12 | ||||||||||||||||
| Sponsor Name:Medical University of Vienna, Department of Medicine III, Division of Nephrology und Dialysis | ||||||||||||||||||
| Full Title: ORAL SODIUM BICARBONATE SUPPLEMENTATION IN PATIENTS WITH CHRONIC METABOLIC ACIDOSIS AND CHRONIC KIDNEY DISEASE | ||||||||||||||||||
| Medical condition: Patients classified to have chronic kidney disease of stage 3 and 4 and chronic metabolic acidosis (venous serum HCO3- of <21mml/L on 2 separate measurements at least 1 day apart) should be include... | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-008745-38 | Sponsor Protocol Number: CKD-VitD-microcirc | Start Date*: 2009-04-08 | ||||||||||||||||
| Sponsor Name:Barts and the London NHS Trust | ||||||||||||||||||
| Full Title: THE EFFECT OF VITAMIN D ON THE MICROCIRCULATION OF PATIENTS WITH CHRONIC KIDNEY DISEASE AND VITAMIN D DEFICIENCY | ||||||||||||||||||
| Medical condition: Chronic kidney disease and vitamin D deficiency. | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2007-004760-49 | Sponsor Protocol Number: MK001 | Start Date*: 2008-01-02 | ||||||||||||||||
| Sponsor Name:University of Dundee | ||||||||||||||||||
| Full Title: Do Xanthine Oxidase Inhibitors reduce both Left Ventricular Hypertrophy and Vascular Dysfunction in Cardiovascular patients with Renal Dysfunction? | ||||||||||||||||||
| Medical condition: Chronic Kidney Disease Stage 3 Left Ventricular Hypertrophy | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-000654-55 | Sponsor Protocol Number: CVD-001 | Start Date*: 2012-08-01 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: Spironolactone to Prevent Cardiovascular Events in Early Stage Chronic Kidney Disease (CKD): A Pilot Trial | |||||||||||||
| Medical condition: chronic kidney disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002721-99 | Sponsor Protocol Number: CT114-2022-01 | Start Date*: 2023-03-28 | |||||||||||
| Sponsor Name:Klinikum Nürnberg | |||||||||||||
| Full Title: Natriuretic-ureothelic adaptation of body fluid homeostasis during SGLT-2 inhibition and/or mineralocorticoid receptor modulation in patients with chronic kidney disease. A 4-arm, double-blind, dou... | |||||||||||||
| Medical condition: Stage 3 chronic kidney disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004888-41 | Sponsor Protocol Number: IPeRStudy | Start Date*: 2012-12-28 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
| Full Title: Intensive Phosphate Control in Development of Renal End Points and Mortality in CKD (the IPeR Study) | |||||||||||||
| Medical condition: Patients with Chronic Kidney Disease (CKD) not yet on dialysis | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-004990-13 | Sponsor Protocol Number: KRM-307 | Start Date*: 2007-10-17 | |||||||||||
| Sponsor Name:Mitsubishi Tanabe Pharma Corporation [...] | |||||||||||||
| Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of AST-120 for Prevention of Chronic Kidney Disease Progression in Patients with Moderate to Severe Chronic Kidney Disease includin... | |||||||||||||
| Medical condition: Moderate to Severe Chronic Kidney Disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001363-31 | Sponsor Protocol Number: M05-741 | Start Date*: 2007-05-28 | |||||||||||
| Sponsor Name:Abbott GmbH & Co KG | |||||||||||||
| Full Title: Estudio VITAL- Estudio del activador del receptor de la vitamina D selectivo (Paricalcitol) para la reducción de la albúmina: Estudio multicéntrico de fase II, prospectivo aleatorizado, a doble cie... | |||||||||||||
| Medical condition: Nefropatía diabética Tipo 2. Type 2 diabetic nephropathy. | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) PT (Completed) GR (Completed) IT (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000773-23 | Sponsor Protocol Number: I4M-MC-MRAC | Start Date*: 2012-04-23 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: Study of the Safety and Efficacy of LY2623091 in Chronic Kidney Disease Patients | |||||||||||||
| Medical condition: Chronic kidney disease | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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