- 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 5 of 14.
EudraCT Number: 2018-004871-11 | Sponsor Protocol Number: ULA02 | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:Cardiorentis AG | |||||||||||||
Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED DOSE ESCALATION STUDY OF ULARITIDE FOLLOWED BY A 42-HOUR INFUSION FOR THE TREATMENT OF ACUTE KIDNEY INJURY (AKI) IN PATIENTS POST CARDIAC SURGERY | |||||||||||||
Medical condition: Acute kidney injury in patients post cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005066-30 | Sponsor Protocol Number: RG_14-088 | Start Date*: 2018-03-20 | |||||||||||
Sponsor Name:The University of Birmingham | |||||||||||||
Full Title: MyeChild 01: International Randomised Phase III Clinical Trial in Children with Acute Myeloid Leukaemia - Incorporating an Embedded Dose Finding Study for Gemtuzumab Ozogamicin in Combination with ... | |||||||||||||
Medical condition: Newly diagnosed acute myeloid leukaemia (AML), high risk myelodysplastic syndrome(MDS) and isolated myeloid sarcoma (either de novo or secondary) are eligible for the trial. | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Trial now transitioned) GB (GB - no longer in EU/EEA) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019638-28 | Sponsor Protocol Number: PMR-EC-1211 | Start Date*: 2010-11-22 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||
Full Title: INVESTIGATING NEW ONSET DIABETES MELLITUS IN KIDNEY TRANSPLANT RECIPIENTS RECEIVING AN ADVAGRAF-BASED IMMUNOSUPPRESSIVE REGIMEN WITH OR WITHOUT CORTICOSTEROIDS – A MULTICENTER, TWO ARM, RANDOMIZED... | |||||||||||||
Medical condition: Prophylaxis of rejection in kidney allograft recipients (by immunosuppression) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) SK (Completed) HU (Completed) ES (Completed) LV (Completed) LT (Completed) EE (Completed) NL (Completed) SE (Completed) IT (Completed) DE (Completed) PT (Completed) BE (Completed) RO (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003288-12 | Sponsor Protocol Number: 02-0-158 | Start Date*: 2015-08-05 | |||||||||||
Sponsor Name:Fujisawa Healthcare, Inc. | |||||||||||||
Full Title: A Phase III, Randomized, Open-Label, Comparative, Multi-Center Study to Assess the Safety and Efficacy of Prograf® (tacrolimus)/MMF, Modified Release (MR) Tacrolimus /MMF and Neoral®(cyclosporin... | |||||||||||||
Medical condition: Kidney transplant recipients | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003818-92 | Sponsor Protocol Number: CURITIBA_TRIAL | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Ospedale San Raffaele, UO Chirurgia Vascolare | |||||||||||||
Full Title: CUstodiol vs RInger: whaT Is the Best Agent? | |||||||||||||
Medical condition: Thoracoabdominal aortic aneurysm | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003733-24 | Sponsor Protocol Number: EPO2008-02 | Start Date*: 2009-05-29 |
Sponsor Name:Abertawe Bro Morgannwg University NHS Trust | ||
Full Title: A randomised study to assess the effects of Epoetin Beta on renal function in patients with critical illness(with or without multi-organ failure) | ||
Medical condition: Sepsis/Acute renal failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000757-49 | Sponsor Protocol Number: QRK309 | Start Date*: 2018-12-05 | |||||||||||
Sponsor Name:Quark Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of QPI-1002 for the Prevention of Major Adverse Kidney Events (MAKE) in Subjects at High Risk for A... | |||||||||||||
Medical condition: QPI-1002 is being developed for prevention of acute kidney injury (AKI) in patients at risk for AKI following cardiac surgery and for reduction in the incidence and severity of delayed graft functi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) BE (Completed) CZ (Completed) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002453-25 | Sponsor Protocol Number: MERCURI-2 | Start Date*: 2023-03-07 | |||||||||||
Sponsor Name:Amsterdam UMC | |||||||||||||
Full Title: Preoperative sodium glucose cotransporter 2 inhibitors for prevention of postoperative acute kidney injury in cardiac surgery patients – a randomized, placebo-controlled, multi-centre, phase IV cli... | |||||||||||||
Medical condition: Cardiac Surgery-Associated Acute Kidney Injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002219-42 | Sponsor Protocol Number: BCX1777-108 | Start Date*: 2009-01-26 | ||||||||||||||||
Sponsor Name:Mundipharma Research Limited | ||||||||||||||||||
Full Title: A Phase I/II Pharmacokinetic Study of Intravenous and Oral Forodesine in Children with Relapsed or Refractory T-cell or B-cell Precursor Acute Lymphoblastic Leukaemia or T-cell Non- Hodgkin’s Lymphoma | ||||||||||||||||||
Medical condition: T-cell or B-cell precursor (BCP) acute lymphoblastic leukaemia (T-ALL or BCP-ALL) or T-cell Non Hodgkin’s lymphoma (T-NHL) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) AT (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002076-41 | Sponsor Protocol Number: 0667 | Start Date*: 2018-08-23 | ||||||||||||||||
Sponsor Name:University of Leicester | ||||||||||||||||||
Full Title: A RANDOMISED CONTROLLED TRIAL OF PRE-SURGERY SODIUM VALPROATE, FOR THE PREVENTION OF ORGAN INJURY IN CARDIAC SURGERY: Val-CARD | ||||||||||||||||||
Medical condition: Reduction of myocardial and kidney injury risk of post cardiac surgery by increasing the expression of genes that promote myocardial mitochondrial homeostasis via effects on chromatin histone deace... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002732-25 | Sponsor Protocol Number: 0105 | Start Date*: 2006-02-01 |
Sponsor Name:Geir Øystein Andersen, Department of Cardiology, Ulleval University Hospital | ||
Full Title: Safety and efficacy of levosimendan in patients with acute myocardial infarction complicated by symptomatic left ventricular failure | ||
Medical condition: Patients with acute myocardial infarction developing acute heart failure after primary PCI (percutaneus coronary intervention). Some patients in a predefined subgroup are categorized as patients in... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000322-66 | Sponsor Protocol Number: CRAD001A2433 | Start Date*: 2013-11-07 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 24 month, multicenter, randomized, open-label safety and efficacy study of concentration-controlled everolimus with reduced calcineurin inhibitor vs mycophenolate with standard calcineurin inhibi... | |||||||||||||
Medical condition: Adult kidney transplant recipients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) SK (Completed) ES (Completed) PT (Completed) AT (Completed) NL (Completed) BE (Completed) GR (Completed) CZ (Completed) SI (Completed) BG (Completed) PL (Completed) HR (Completed) NO (Completed) SE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019639-37 | Sponsor Protocol Number: PMR-EC-1212 | Start Date*: 2011-10-10 | |||||||||||
Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||
Full Title: A MULTICENTER, TWO ARM, RANDOMIZED, OPEN LABEL CLINICAL STUDY INVESTIGATING RENAL FUNCTION IN AN ADVAGRAF-BASED IMMUNOSUPPRESSIVE REGIMEN WITH OR WITHOUT SIROLIMUS IN KIDNEY TRANSPLANT SUBJECTS. | |||||||||||||
Medical condition: Prophylaxis of rejection in kidney allograft recipients (by immunosuppression) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) AT (Completed) DE (Completed) ES (Completed) SK (Prematurely Ended) NL (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003497-48 | Sponsor Protocol Number: EMPATHY | Start Date*: 2021-11-29 | |||||||||||
Sponsor Name:Medical University of Warsaw | |||||||||||||
Full Title: Empagliflozin and dapagliflozin in patients hospitalized for acute decompensated heart failure (EMPATHY) – a phase III trial | |||||||||||||
Medical condition: acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003001-85 | Sponsor Protocol Number: BDD | Start Date*: 2005-11-28 |
Sponsor Name:Austrian Forum against Cancer | ||
Full Title: Bortezomib-Doxorubicin-Dexamethasone (BDD) as Treatment for Patients with Multiple Myeloma Presenting with Acute Renal Failure | ||
Medical condition: The occurrence of renal failure is an emergency situation in patients with multiple myeloma. A fast active relatively, non-toxic protocol seems presently the best option for attempts to reverse ren... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) CZ (Completed) HU (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002882-20 | Sponsor Protocol Number: | Start Date*: 2019-04-17 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A multicentre randomised controlled trial to assess the safety and efficacy of adding rituximab to standard of care in treating acute antibody-mediated rejection in kidney transplantation (Transpla... | |||||||||||||
Medical condition: Renal Transplant antibody-mediated rejection | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004540-23 | Sponsor Protocol Number: CAEB071A2206 | Start Date*: 2007-07-17 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A 12-month open-label, randomized, multicenter, sequential cohort, dose finding study to evaluate the efficacy, safety and tolerability of oral AEB071 versus Neoral® in combination with Certican®, ... | ||
Medical condition: renal transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) AT (Completed) IT (Completed) FR (Completed) BE (Completed) NL (Completed) SK (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000983-41 | Sponsor Protocol Number: ID-076A301 | Start Date*: 2021-11-03 | |||||||||||
Sponsor Name:Idorsia Pharmaceuticals Ltd | |||||||||||||
Full Title: Multi-center, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the efficacy and safety of self-administered subcutaneous selatogrel for prevention of all-cause death a... | |||||||||||||
Medical condition: Acute myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) SK (Trial now transitioned) DK (Trial now transitioned) EE (Trial now transitioned) LT (Trial now transitioned) ES (Ongoing) AT (Trial now transitioned) BG (Trial now transitioned) FR (Trial now transitioned) NO (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) CZ (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) NL (Trial now transitioned) IE (Prematurely Ended) GR (Trial now transitioned) PT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002345-23 | Sponsor Protocol Number: A3921050 | Start Date*: 2008-11-28 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY10017, USA | |||||||||||||
Full Title: A PHASE 2, MULTICENTER, OPEN-LABEL, ACTIVE COMPARATOR CONTROLLED, EXTENSION TRIAL TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF CP-690,550 IN RENAL ALLOGRAFT RECIPIENTS | |||||||||||||
Medical condition: Prevention of kidney allograft rejection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) PT (Completed) BE (Completed) NL (Completed) IT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003025-22 | Sponsor Protocol Number: 18IA31 | Start Date*: 2019-12-22 | ||||||||||||||||
Sponsor Name:Great Ormond Street Hospital for Children NHS Foundation Trust | ||||||||||||||||||
Full Title: PlasmaLyte Usage and assessment of kidney Transplant Outcomes in children: the PLUTO trial | ||||||||||||||||||
Medical condition: Kidney transplantation in paediatric patients with end-stage kidney disease | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
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