- Trials with a EudraCT protocol (5,163)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (12)
5,163 result(s) found for: Renal Disease.
Displaying page 2 of 259.
| EudraCT Number: 2008-006014-20 | Sponsor Protocol Number: FARM6X822T | Start Date*: 2009-01-19 | |||||||||||
| Sponsor Name:CONSORZIO MARIO NEGRI SUD | |||||||||||||
| Full Title: Effects of the dose of erythropoiesis stimulating agents on cardiac-cerebrovascular outcomes and quality of life in hemodialysis patients. The DOSe of Erythropoietins (DOSE) trial. | |||||||||||||
| Medical condition: End stage kidney disease and anemia, treated with hemodialysis for renal replacement therapy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-016362-85 | Sponsor Protocol Number: ST1472-DM-09-005 | Start Date*: 2009-11-09 | |||||||||||
| Sponsor Name:SIGMA-TAU | |||||||||||||
| Full Title: A PILOT, RANDOMIZED, SINGLE SITE, 3 PARALLEL ARMS, OPEN-LABEL STUDY IN PATIENTS ON CHRONIC DIALYSIS WITH END STAGE RENAL DISEASE (ESRD) TO EVALUATE THE ENHANCING EFFECT OF TWO DOSES OF THYMOSIN ALP... | |||||||||||||
| Medical condition: ZADAXIN ENHANCING EFFECT IN PATIENTS ON CHRONIC DIALYSIS WITH END STAGE RENAL DISEASE (ESRD) TREATED WITH EGG-DERIVED H1N1sw MONOVALENT INFLUENZA VACCINE | |||||||||||||
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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: 2010-020114-29 | Sponsor Protocol Number: IGFHD1-2010 | Start Date*: 2010-07-13 | |||||||||||
| Sponsor Name:Department of Nephrology | |||||||||||||
| Full Title: Insulin-like growth factor in hemodialysis patients | |||||||||||||
| Medical condition: This project aims to investigate whether the anabolic potentials of insulin may be used to reverse the catabolic effects of hemodialysis in non-diabetic patients with end-stage renal failure. Thus... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2009-016531-35 | Sponsor Protocol Number: SPD405-703 | Start Date*: 2010-05-18 | |||||||||||
| Sponsor Name:Shire Pharmaceutical Development Ltd | |||||||||||||
| Full Title: A Proof of Concept, Phase 2a, Double-blind, Parallel Group, Randomised, Placebo controlled Study to Assess the Effect of Lanthanum Carbonate on intact FGF23 in Normo-phosphataemic Subjects with Sta... | |||||||||||||
| Medical condition: Chronic Kidney Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000431-40 | Sponsor Protocol Number: UF9672 | Start Date*: 2016-05-19 | |||||||||||
| Sponsor Name:Health Ministry | |||||||||||||
| Full Title: Randomized controlled study evaluating the effect of a biotherapy treatment (anti-RANKL ligand antibody: Denosumab) on bone and vascular metabolism in osteoporotic chronic kidney disease | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Elderly | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004618-42 | Sponsor Protocol Number: RISO06 | Start Date*: 2006-09-25 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA PROVINCIALE DI LECCO | |||||||||||||
| Full Title: An evaluation of sodium removal with some peritoneal solutions a pilot study | |||||||||||||
| Medical condition: end stage renal disease | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| 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: 2004-001390-26 | Sponsor Protocol Number: PRO-RENAL-REG-064 | Start Date*: 2004-11-09 | |||||||||||
| Sponsor Name:Baxter R&D Europe SCRL | |||||||||||||
| Full Title: A Subjective Evaluation of Inflow Pain: Comparison of Extraneal to Extraneal Physiological pH | |||||||||||||
| Medical condition: Patients with End Stage Renal Disease (ESRD) undergoing peritoneal dialysis (PD) therapy and experiencing pain on infusion with Extraneal not related to the catheter or volume of dialysis fluid. | |||||||||||||
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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: 2010-018838-45 | Sponsor Protocol Number: RLY5016–204 | Start Date*: 2010-04-21 | ||||||||||||||||
| Sponsor Name:Relypsa, Inc. | ||||||||||||||||||
| Full Title: A Multicenter, Open-Label, Single-Arm Study to Evaluate a Titration Regimen for RLY5016 in Heart Failure Patients with Chronic Kidney Disease | ||||||||||||||||||
| Medical condition: Heart failure with Chronic kidney disease | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SI (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| 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: 2009-011497-15 | Sponsor Protocol Number: CERA | Start Date*: 2009-05-07 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
| Full Title: PILOT CLINICAL TRIAL WITH MIRCERA (methoxy polyethylene glycol-epoetin beta) IN DIALYSIS UNIT OF A.O. SAN GIOVANNI BATTISTA DI TORINO | |||||||||||||
| Medical condition: End stage renal patients in hemodialysis or peritoneal dialysis treatment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| 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: 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: 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: 2007-006606-16 | 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: 2020-002192-35 | Sponsor Protocol Number: 19225 | Start Date*: 2020-10-13 | |||||||||||
| Sponsor Name:Bayer - AG | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, multi-center study to assess the efficacy and safety of BAY 2327949 in patients with chronic kidney disease (eGFR range from 25 to 60 mL/min/1.73 m²)... | |||||||||||||
| Medical condition: Chronic Kidney Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) NO (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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