- Trials with a EudraCT protocol (4,530)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (30)
4,530 result(s) found for: Renal function.
Displaying page 1 of 227.
EudraCT Number: 2008-004099-26 | Sponsor Protocol Number: 6.version,september2011 | Start Date*: 2009-12-10 | ||||||||||||||||
Sponsor Name:Departmnet of nephrology | ||||||||||||||||||
Full Title: Randomised trial on combined effects of dual blockade of the renin angiotensin system and phosphate binding in diabetic and non-diabetic patients with impaired renal function. | ||||||||||||||||||
Medical condition: decreased renal function (CKD II-IV), creatinin clearance 15-90 ml/min | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000995-13 | Sponsor Protocol Number: DECODE-CKD | Start Date*: 2022-01-26 | |||||||||||
Sponsor Name:Department of Cardiology, Herlev and Gentofte hospital | |||||||||||||
Full Title: A 6-Month, Randomized, Double-Blind Study to Evaluate the Effect of Dapagliflozin on EChOcardiographic Measures of CarDiac StructurE and Function in Patients with Chronic Kidney Disease (DECODE-CKD) | |||||||||||||
Medical condition: Chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2008-008246-20 | Sponsor Protocol Number: ABR 25995 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Center, Department of Anaesthesiology, Pain and Palliative Medic | |||||||||||||||||||||||
Full Title: Evaluation of the efficacy and safety of sugammadex (Bridion) in children with renal failure. | |||||||||||||||||||||||
Medical condition: Sugammadex is a selective relaxant binding agent, which is administered in case of a rocuronium-induced neuromuscular block, during general anaesthesia. The aim of the trial is to investigate the u... | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003496-29 | Sponsor Protocol Number: I13034 | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:University Hospital, Limoges | |||||||||||||
Full Title: Designing a Bayesian model of the plasma clearance of Calcium edetate de sodium, with a limited sampling strategy for the calculation of Glomerular Filtration Rate (GFR) and validity assessment com... | |||||||||||||
Medical condition: Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001407-11 | Sponsor Protocol Number: Certican MHH PRTx01 | Start Date*: 2006-07-18 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: A single center study investigating ciclosporine A microemulsion in combination with basiliximab and prednisolon and switch to low-dose ciclosporine A and everolimus without steroids in the prevent... | |||||||||||||
Medical condition: Kidney transplantation after end stage renal failure | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (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: 2011-002586-38 | Sponsor Protocol Number: RPH-1101 | Start Date*: 2011-10-14 | |||||||||||
Sponsor Name:Renapharma AB | |||||||||||||
Full Title: A 12-week clinical double-blind, randomised study of cholecalciferol versus placebo in patients with chronic kidney disease stage 3-4 (CHICK). | |||||||||||||
Medical condition: Chronic renal failure, stage 3-4 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000948-98 | Sponsor Protocol Number: H-3-2011-154 | Start Date*: 2012-05-03 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of epinephrine on systemic absorption of mepivacaine administered for brachial plexus block in patients with end-stage renal disease | |||||||||||||
Medical condition: End-stage renal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000606-75 | Sponsor Protocol Number: IP-001-06 | Start Date*: 2007-03-27 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Assessment of dialytic efficacy and tolerability of a peritoneal dialysis solution for notturnal exchange containing L-Carnitine in End Stage Renal Disease Patients (ESRD) in Automatised Peritonea... | |||||||||||||
Medical condition: Utilization of a peritoneal solution containing L-Carnitine as osmotic agent in the treatment of ESRD patients with APD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2022-002684-29 | Sponsor Protocol Number: IP-001-21 | Start Date*: 2023-07-10 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA S.R.L. | |||||||||||||
Full Title: A Study of GlucoThera Plus for PeRitoneal DiAlysis in Children. | |||||||||||||
Medical condition: End-Stage Renal Disease (ESRD) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019243-19 | Sponsor Protocol Number: 004-09 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Angion Biomedica Corp. | |||||||||||||
Full Title: Pilot Study of BB3 to Improve Renal Function in Patients with Signs and Symptoms of Significant Renal Injury after Kidney Transplantation from Donors after Cardiac Death | |||||||||||||
Medical condition: Patients suffering from end-stage renal disease, receiving a donor kidney from donors after cardiac death | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 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: 2008-003727-23 | Sponsor Protocol Number: RRK3563 | Start Date*: 2008-12-16 | |||||||||||
Sponsor Name:University Hospital Birmingham NHS Foundation Trust | |||||||||||||
Full Title: Does phosphate binding with sevelamer carbonate improve cardiovascular structure and function in patients with early chronic kidney disease? | |||||||||||||
Medical condition: Chronic kidney disease stage 3 (eGFR 30-59 ml/min/1.73m2) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012445-35 | Sponsor Protocol Number: ALBLOCK-2 | Start Date*: 2009-11-26 | |||||||||||
Sponsor Name:Herlev Hospital | |||||||||||||
Full Title: Aldosterone receptor blockade in patients with chronic kidney disease. Influence on arterial stiffness and kidney function. | |||||||||||||
Medical condition: Chronic kidney disease, stages 3 and 4. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000410-37 | Sponsor Protocol Number: 310107 | Start Date*: 2007-09-26 | |||||||||||
Sponsor Name:University Of Tuebingen | |||||||||||||
Full Title: Determination of glomerular filtration rate (GFR) using MR nephrography in patients with chronic kidney disease. | |||||||||||||
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: 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: 2014-001778-32 | Sponsor Protocol Number: U1111-1149-7801 | Start Date*: 2014-08-12 | |||||||||||||||||||||
Sponsor Name:Bo Feldt-Rasmussen | |||||||||||||||||||||||
Full Title: Glycaemic and cardiovascular efficacy of liraglutide in prediabetic patients with end-stage renal disease | |||||||||||||||||||||||
Medical condition: Prediabetes and dialysis dependent end-stage renal disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
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