- 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 9 of 14.
EudraCT Number: 2006-005687-44 | Sponsor Protocol Number: 0468H1-316 | Start Date*: 2015-04-10 |
Sponsor Name:Wyeth Research | ||
Full Title: A Randomized, Open-Label, Comparative Evaluation of Conversion From Calcineurin Inhibitors to Sirolimus Versus Continued Use of Calcineurin Inhibitors in Renal Allograft Recipients | ||
Medical condition: Renal Transplantation | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2013-000819-25 | Sponsor Protocol Number: 43712 | Start Date*: 2013-10-22 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Autologous BM derived MSCs in combination with everolimus to preserve renal structure and function in renal recipients | ||
Medical condition: renal recipients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013220-24 | Sponsor Protocol Number: | Start Date*: 2009-11-02 | |||||||||||
Sponsor Name:Addenbrooke's Hospital | |||||||||||||
Full Title: Plasma Exchange and Glucocorticoid Dosing in the Treatment of Anti-neutrophil Cytoplasm Antibody Associated Vasculitis: an International Randomised Controlled Trial | |||||||||||||
Medical condition: ANCA associated vasculitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) IT (Completed) SE (Completed) DK (Completed) CZ (Completed) ES (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024381-21 | Sponsor Protocol Number: CRAD001A2314 | Start Date*: 2011-07-29 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12-month, multicenter, open label, randomized, controlled study to evaluate the efficacy, tolerability and safety of early introduction of everolimus, reduced CNI, and early steroid elimination c... | |||||||||||||
Medical condition: Prevention of acute rejection in paediatric recipients of a renal transplant | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) FR (Completed) DE (Completed) NO (Completed) IT (Completed) Outside EU/EEA SE (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005635-10 | Sponsor Protocol Number: ATEGE_LIVER | Start Date*: 2006-05-22 |
Sponsor Name:Liver Unit, ICMD, Hospital Clinic Barcelona | ||
Full Title: INDUCTION TREATMENT FOLLOWED BY IMMUNOSUPPRESSION WITHDRAWAL IN LIVER TRANSPLANTATION: A COMPARATIVE TRIAL. Tratamiento de inducción y retirada de la inmunosupresión en el trasplante hepático. Estu... | ||
Medical condition: Liver transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001320-34 | Sponsor Protocol Number: 2020-6384 | Start Date*: 2020-04-10 |
Sponsor Name:Radboudumc | ||
Full Title: A double-blind, placebo-controlled randomized clinical trial with valsartan for PRevention of Acute rEspiraTORy dIstress syndrome in hospitAlized patieNts with SARS-COV-2 Infection Disease | ||
Medical condition: SARS-CoV-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-000997-39 | Sponsor Protocol Number: 7837 | Start Date*: 2018-03-09 | |||||||||||
Sponsor Name:Newcastle Upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Eculizumab in Shiga-Toxin producing E. Coli Haemolytic Uraemic Syndrome (ECUSTEC): A Randomised, Double-Blind, Placebo-Controlled Trial | |||||||||||||
Medical condition: Shiga-toxin producing E. Coli Haemolytic Uraemic Syndrome (STEC HUS) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001178-20 | Sponsor Protocol Number: IM103-307,SMR-2729 | Start Date*: 2013-10-29 | |||||||||||
Sponsor Name:Uppsala University Hospital, MHT, Department of Nephrology | |||||||||||||
Full Title: Cardiovascular (CV) risk prediction and CV biomarkers in renal transplant recipients treated with belatacept compared to calcineurin inhibitors (CNI). Open randomized 12 month study. | |||||||||||||
Medical condition: Prophylaxis of graft rejection in adults who have received a renal transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003603-33 | Sponsor Protocol Number: SIGMA4COVID | Start Date*: 2021-01-14 |
Sponsor Name:Consorci Mar Parc de Salut de Barcelona | ||
Full Title: Efficacy of E-52862 in the early treatment of confirmed mild symptomatic COVID-19 patients | ||
Medical condition: Patients with mild COVID-19 disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003240-11 | Sponsor Protocol Number: LCP-Tacro 3001 | Start Date*: 2009-02-25 | |||||||||||
Sponsor Name:LifeCycle Pharma A/S | |||||||||||||
Full Title: A Phase 3, Open-label, Multicenter, Prospective, Randomized Study of the Efficacy and Safety of Conversion from Prograf® Capsules Twice Daily to LCP-Tacro™ Tablets Once Daily for the Prevention of ... | |||||||||||||
Medical condition: LCP-Tacro tablets will be investigated for immunosuppression for the prevention of acute allograft rejection in adult renal transplant patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001245-13 | Sponsor Protocol Number: 4LB-LEO-P | Start Date*: 2022-03-03 | ||||||||||||||||
Sponsor Name:4Living Biotech SAS | ||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, two parallel groups, international multicenter trial to evaluate the effect of Plerixafor in acute respiratory failure related to COVID-19 (LEONARDO) | ||||||||||||||||||
Medical condition: Severe COVID-19 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) NL (Prematurely Ended) BG (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001620-33 | Sponsor Protocol Number: APHP200033 | Start Date*: 2021-01-13 |
Sponsor Name:ASSISTANCE-PUBLIQUE HOPITAUX DE PARIS (AP-HP) | ||
Full Title: HYdrocortisone and VAsopressin in Post-RESuscitation Syndrome | ||
Medical condition: Adult cardiac arrest patients with sustained ROSC and hemodynamic failure due to post-resuscitation syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000224-35 | Sponsor Protocol Number: RECEM00001 | Start Date*: 2021-07-28 | |||||||||||
Sponsor Name:Marie Kristine Jessen | |||||||||||||
Full Title: Restrictive Fluid Administration vs. Standard of Care in Emergency Department Sepsis Patients - a Multicenter, Randomized Clinical Feasibility Trial | |||||||||||||
Medical condition: Sepsis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005144-14 | Sponsor Protocol Number: 01-CARDIONIDO | Start Date*: 2018-04-12 |
Sponsor Name:Dr. Forteza Gil | ||
Full Title: Comparative study of two types of cardioplegia during cardiac surgery in the adult patient | ||
Medical condition: Cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023920-26 | Sponsor Protocol Number: PREV-ARA | Start Date*: 2011-02-09 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica Hospital Universitario Ramón y Cajal | |||||||||||||
Full Title: Eficacia y seguridad del bicarbonato en el tratamiento de la alteración renal aguda asociada a la cirugía cardiaca | |||||||||||||
Medical condition: Alteración renal aguda, término recomendado para traducir acute kidney injury que en los últimos años ha sustituido en la literatura internacional al término acute renal failure, habitualmente trad... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004549-35 | Sponsor Protocol Number: CONCHAA | Start Date*: 2021-05-13 |
Sponsor Name:University Hospital Of Araba | ||
Full Title: Usefulness of the use of N-Acetylcysteine associated with conventional treatment in patients with severe alcoholic hepatitis (Maddrey> = 32) | ||
Medical condition: Alcoholic hepatitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-004207-32 | Sponsor Protocol Number: TIKTAC-2-Trial | Start Date*: 2023-04-20 |
Sponsor Name:Medical University Innsbruck, Internal Medicine V | ||
Full Title: Daratumumab in combination with Carfilzomib, Pomalidomide and Dexamethasone (DCPD) in patients with multiple myeloma induced acute renal failure NOT requiring dialysis - “Time Is Kidney in the Trea... | ||
Medical condition: Multiple Myeloma: Patients with MM are frequently diagnosed primarily due to renal failure. Patients with renal failure have a poor prognosis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003563-38 | Sponsor Protocol Number: 20140159 | Start Date*: 2015-04-21 | |||||||||||
Sponsor Name:Amgen, Inc. | |||||||||||||
Full Title: A Multicenter Single-arm Extension Study to Characterize the Long-term Safety of Cinacalcet Hydrochloride in the Treatment of Secondary Hyperparathyroidism in Pediatric Subjects With Chronic Kidn... | |||||||||||||
Medical condition: Secondary Hyperparathyroidism and Chronic Kidney Disease Receiving Dialysis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) HU (Completed) CZ (Completed) ES (Completed) BE (Completed) SK (Completed) FR (Completed) Outside EU/EEA GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002871-36 | Sponsor Protocol Number: VIR-7831-5001 | Start Date*: 2020-11-27 | ||||||||||||||||
Sponsor Name:Vir Biotechnology, Inc. | ||||||||||||||||||
Full Title: A randomized, multi-center, double-blind, placebo-controlled study to assess the safety and efficacy of monoclonal antibody VIR-7831 for the early treatment of coronavirus disease 2019 (COVID-19) i... | ||||||||||||||||||
Medical condition: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection, the cause of coronavirus disease 2019 (COVID-19) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001899-32 | Sponsor Protocol Number: RESINFENOL | Start Date*: 2017-08-17 |
Sponsor Name:Dr. Abelardo Aguilera Peralta | ||
Full Title: Crossover and randomized clinical trial on the effect of Resincolestiramine in the intestinal absorption of new uremic toxins in patients in hemodialysis with chronic renal insufficiency | ||
Medical condition: Chronic renal insufficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
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