- Trials with a EudraCT protocol (261)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
261 result(s) found for: Acute kidney failure.
Displaying page 3 of 14.
EudraCT Number: 2023-000010-18 | Sponsor Protocol Number: WATERLAND | Start Date*: 2023-03-23 | |||||||||||
Sponsor Name:Enrique de Madaria | |||||||||||||
Full Title: Normal saline versus lactated Ringer’s solution for acute pancreatitis resuscitation, an open-label multicenter randomized controlled trial: the WATERLAND trial | |||||||||||||
Medical condition: Acute pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004346-40 | Sponsor Protocol Number: CRAD001A2418 | Start Date*: 2005-05-02 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Full title of the trial : Multi-center, open-label, prospective, randomized, parallel group study investigating a CNI-free regimen with Myfortic® and Certican® in comparison to standard therapy wit... | |||||||||||||
Medical condition: de novo kidney transplantation (cadaveric, living unrelated or living related) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000726-11 | Sponsor Protocol Number: SHP616-302 | Start Date*: 2016-03-08 | |||||||||||
Sponsor Name:Shire Viropharma, Inc. | |||||||||||||
Full Title: A randomized double-blind placebo-controlled study to evaluate the efficacy and safety of Cinryze® (C1 esterase inhibitor [human]) for the treatment of acute antibody-mediated rejection in kidney t... | |||||||||||||
Medical condition: Acute Antibody Mediated Rejection (AMR) in kidney transplant patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002026-78 | Sponsor Protocol Number: GRASPA-AML-2012-01 | Start Date*: 2014-02-26 | |||||||||||
Sponsor Name:ERYTECH Pharma | |||||||||||||
Full Title: A Multicentre, open, randomized, controlled phase IIb trial evaluating efficacy and tolerability of GRASPA (L-asparaginase encapsulated in red blood cells) plus low-dose cytarabine vs low-dose cyta... | |||||||||||||
Medical condition: Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) FI (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005055-33 | Sponsor Protocol Number: ML17443 | Start Date*: 2005-09-01 | |||||||||||
Sponsor Name:Barts and the London NHS Trust | |||||||||||||
Full Title: Evaluating the safety and efficacy of mycophenolate mofetil, daclizumab and a single, initial week of corticosteroids in combination with tacrolimus or sirolimus with continued steroid as mainstay ... | |||||||||||||
Medical condition: Renal Transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003254-24 | Sponsor Protocol Number: | Start Date*: 2019-07-03 |
Sponsor Name:University Hospitals Birmingham NHS Foundation Trust | ||
Full Title: AGe-adapted benefits of Envarsus versus twice-daily tacrolimus ImmunosuppressioN druGs after kidney transplantation (AGEING) – a feasibility study | ||
Medical condition: Immunosuppression in Renal transplant | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004956-39 | Sponsor Protocol Number: SMART-DSA | Start Date*: 2014-06-18 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: Study to evaluate the impact of donor-specific HLA-antibodies on graft function and survival after renal transplantation - Long term follow up of the SMART study population | |||||||||||||
Medical condition: Renal Transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002695-45 | Sponsor Protocol Number: 15-156 | Start Date*: 2018-05-16 |
Sponsor Name:RWTH Aachen University represented by the Rector, himself, represented by the Dean of the Medical Faculty | ||
Full Title: Effect of Empagliflozin on Cardiac Output in Patients with Acute Heart Failure (EMPA Acute Heart Failure) | ||
Medical condition: Patients with acute heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-000484-86 | Sponsor Protocol Number: 02022018 | Start Date*: 2019-01-16 | |||||||||||||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||||||||||||
Full Title: DAN-WAR-D Danish Warfarin-Dialysis Study Safety and efficacy of warfarin in patients with atrial fibrillation on dialysis - A nationwide parallel-group open randomized clinical trial | |||||||||||||||||||||||
Medical condition: Atrial fibrillation, end-stage renal disease, and stroke | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003105-25 | Sponsor Protocol Number: MiLe-1 | Start Date*: 2014-08-27 |
Sponsor Name:Sahlgrenska University Hospital / The Queen Silvia Children´s Hospital | ||
Full Title: The prophylactic effect of levosimendan in reducing acute kidney injury postoperatively in pediatric patients undergoing corrective heart surgery | ||
Medical condition: Acute kidney injury postoperatively in connection with surgery for congenital heart disease | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000837-39 | Sponsor Protocol Number: CCD01 | Start Date*: 2007-08-15 | |||||||||||
Sponsor Name:Cytonet GmbH & Co. KG | |||||||||||||
Full Title: Open, randomized, prospective, controlled, multicentre study to evaluate the efficacy and safety of multiple intraportal applications of liver cell suspension in patients with acute liver failure n... | |||||||||||||
Medical condition: Acute Liver Failure Subgroups of patients with indications falling under ICD classification codes:K70.4, K71, K72, K75, K76, K77 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004301-24 | Sponsor Protocol Number: ONErgt11 | Start Date*: 2012-01-05 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Free State of Bavaria, represented by the University of Regensburg, represented by Prof. Edward K. Geissler | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The ONE Study: A Unified Approach to Evaluating Cellular Immunotherapy in Solid Organ Transplantation – Reference Group Trial | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Kidney allograft rejection following living-donor renal transplantation. | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) IT (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000561-33 | Sponsor Protocol Number: TOL-2 | Start Date*: 2022-03-08 | |||||||||||
Sponsor Name:TolerogenixX GmbH | |||||||||||||
Full Title: An open, randomized-controlled, multi-center phase-II clinical trial of individualized immunosuppression with intravenously administered donor modified immune cells (MIC) compared to standard-of-ca... | |||||||||||||
Medical condition: Living donor kidney transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002168-17 | Sponsor Protocol Number: BAY94-8862/16275 | Start Date*: 2015-12-09 | |||||||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||||||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, double-dummy, parallel-group, active-controlled study to evaluate the efficacy and safety of finerenone compared to eplerenone on morbidity and mortality in... | |||||||||||||||||||||||||||||||||
Medical condition: Subjects with chronic heart failure and reduced ejection fraction after recent heart failure decompensation and additional risk factors, either type 2 diabetes mellitus or chronic kidney disease or... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) IE (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) PT (Prematurely Ended) ES (Prematurely Ended) LT (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004301-41 | Sponsor Protocol Number: P170404J | Start Date*: 2018-10-15 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS [...] | |||||||||||||
Full Title: FURosemide Stress Test to predict need of Renal Replacement THERapy in Ischemic Acute Tubular Necrosis in Intensive Care Units | |||||||||||||
Medical condition: FURosemide Stress Test to predict need of Renal Replacement THERapy in Ischemic Acute Tubular Necrosis in Intensive Care Units | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001455-39 | Sponsor Protocol Number: OPN-305-102 | Start Date*: 2012-10-10 | |||||||||||
Sponsor Name:Opsona Therapeutics Ltd | |||||||||||||
Full Title: A Three-Part, Multi-Centre, Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Sequential Adaptive, Phase II Study to Evaluate the Safety, Tolerability and Efficacy of OPN-305, a Humanis... | |||||||||||||
Medical condition: Prevention of Kidney Graft Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) NL (Completed) GB (Completed) CZ (Completed) AT (Completed) ES (Ongoing) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003023-20 | Sponsor Protocol Number: UCL-PLTP-002 | Start Date*: 2008-09-11 | |||||||||||
Sponsor Name:Cliniques universitaires Saint-Luc | |||||||||||||
Full Title: TACROLIMUS – DACLIZUMAB - MYCOPHENOLATE MOFETIL IMMUNE PROPHYLAXIS IN PEDIATRIC LIVER TRANSPLANTATION. An open, pilot, investigator-driven study in 20 recipients | |||||||||||||
Medical condition: Liver transplantation | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003589-25 | Sponsor Protocol Number: Levo-AKI | Start Date*: 2014-11-11 |
Sponsor Name:Sahlgrenska Universitetssjukhuset/Sahlgrenska | ||
Full Title: The effect of levosimendan, on renal blood flow, function and oxygen uptake during acute renal failure after cardiac surgery | ||
Medical condition: Acute kidney injury postoperatively in connection with heart surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003633-32 | Sponsor Protocol Number: CERL080A2419 | Start Date*: 2006-11-13 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, multi-center, parallel-group, open-label study to evaluate the therapeutical benefit of an initially intensified dosing regimen of Myfortic® vs. a standard dosing regimen of Myfortic... | ||
Medical condition: Prophylaxis of rejection in recipients of first or second cadaveric, living unrelated or living related kidney transplants | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) AT (Completed) IT (Completed) SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000925-36 | Sponsor Protocol Number: CCFZ533X2201 | Start Date*: 2015-11-26 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12-month randomized, multiple dose, open-label, study evaluating safety, tolerability, pharmacokinetics/pharmacodynamics (PK/PD) and efficacy of an anti-CD40 monoclonal antibody, CFZ533, in combi... | |||||||||||||
Medical condition: acute rejection of renal transplant in de novo adult renal transplant patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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