- Trials with a EudraCT protocol (2,038)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
2,038 result(s) found for: Renal clearance.
Displaying page 1 of 102.
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: 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: 2015-000856-16 | Sponsor Protocol Number: DTG_HD | Start Date*: 2015-05-27 | ||||||||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | ||||||||||||||||||
Full Title: Removal of dolutegravir by hemodialysis in HIV-infected patients with end-stage renal disease. | ||||||||||||||||||
Medical condition: HIV-infected patients with end-stage renal disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (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: 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: 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: 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: 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: 2006-005298-23 | Sponsor Protocol Number: IP-002-05 | Start Date*: 2007-03-12 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Efficiency of L-Carnitine-containing Peritoneal Dialysis Solutions for diurnal exchanges in CAPD Patients with ESRD on Glucose and Lipid Metabolisms. Randomized, Parallel Study Compared versus a St... | |||||||||||||
Medical condition: Patients affected by End stage renal disease ESRD treated with Continuous Ambulatory Peritoneal Dialysis CAPD . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001388-23 | Sponsor Protocol Number: PRO-RENAL-REG-062 | Start Date*: 2004-11-09 | |||||||||||
Sponsor Name:Baxter R&D Europe SCRL | |||||||||||||
Full Title: A Study to Evaluate the Efficacy and Safety of Extraneal Physiological pH Compared with Current Extraneal in Patients Receiving Continuous Ambulatory Peritoneal Dialysis (CAPD). | |||||||||||||
Medical condition: End Stage Renal Disease patients receiving continuous ambulatiry peritoneal dialysis (CAPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005300-13 | Sponsor Protocol Number: IP-003-05 | Start Date*: 2007-05-29 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Efficiency of L-Carnitine-containing Peritoneal Dialysis Solutions for diurnal exchanges in diabetes type 2 CAPD patients with ESRD on glucose metabolism. Randomized, parallel study compared versus... | |||||||||||||
Medical condition: Patients affected by End Stage Renal Disease (ESRD) treated with Continuous Ambulatory Peritoneal Dialysis (CAPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (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: 2019-004152-10 | Sponsor Protocol Number: EMPATHY | Start Date*: 2020-01-30 | ||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||
Full Title: Evaluating the Short-Term Renal and Systemic Effects of SGLT2 Inhibition in Non-Diabetic Patients at Risk of Accelerated GFR Decline Because of Glomerular Hyperfiltration: a sequential OFF-ON-OFF S... | ||||||||||||||||||
Medical condition: Obesity Renal chronic disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
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: 2004-000457-34 | Sponsor Protocol Number: FG-506-02-40 | Start Date*: 2004-10-19 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: A MULTICENTRE, RANDOMISED, OPEN CLINICAL STUDY TO COMPARE THE EFFICACY AND SAFETY OF A COMBINATION THERAPY OF TACROLIMUS WITH SIROLIMUS VERSUS TACROLIMUS WITH MYCOPHENOLATE MOFETIL IN KIDNEY TRANSP... | |||||||||||||
Medical condition: Patients with end stage kidney disease who will undergo primary renal transplantation or retransplantation. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) AT (Completed) ES (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2005-004989-17 | Sponsor Protocol Number: KRM-306 | 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 | |||||||||||||
Medical condition: Moderate to Severe Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) IT (Completed) | |||||||||||||
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: 2012-000773-23 | 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 |
EudraCT Number: 2007-003866-16 | Sponsor Protocol Number: AP REN 01-01 | Start Date*: 2009-03-03 | ||||||||||||||||
Sponsor Name:AM-Pharma B.V. | ||||||||||||||||||
Full Title: A Phase-II, double-blind, randomized, placebo-controlled proof of concept study on the safety and early efficacy of Alkaline Phosphatase in sepsis patients with Renal Failure. | ||||||||||||||||||
Medical condition: Sepsis with Renal Failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
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