- Trials with a EudraCT protocol (684)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
684 result(s) found for: Terminal disease.
Displaying page 2 of 35.
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: 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: 2009-012445-35 | 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: 2020-001033-12 | 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: 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: 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: 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: 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: 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: 2011-002640-27 | Sponsor Protocol Number: GED-301-01-11 | Start Date*: 2011-07-14 | |||||||||||
Sponsor Name:GIULIANI | |||||||||||||
Full Title: A phase II multicenter, randomized, double-blind, controlled vs placebo, dose-finding study on the efficacy and safety of GED-0301, in patients with active Crohn‟s disease (Ileo-Colitis) | |||||||||||||
Medical condition: ACTIVE CROHN'S DISEASE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 2005-005658-37 | Sponsor Protocol Number: 2006-1 | Start Date*: 2006-07-07 | |||||||||||
Sponsor Name:Dpt. of Urology -K. Aarhus University Hospital | |||||||||||||
Full Title: A randomized, multi-center study to assess the effect of Darbepoetin alfa (Aranesp®) for the treatment of anemia in patients with advanced hormone independent prostate cancer and anaemia | |||||||||||||
Medical condition: In an open randomised, multi-center study to identify the haematopoietic response to Aranesp® (Darbepoetin 6,75 mcg/kg) administrated every fourth week compared to standard care of treatment in pat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (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 |
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