- Trials with a EudraCT protocol (161)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
161 result(s) found for: Acute Kidney Injury.
Displaying page 2 of 9.
EudraCT Number: 2022-003000-32 | Sponsor Protocol Number: ACTRN12619001355167 | Start Date*: 2023-06-23 | |||||||||||||||||||||
Sponsor Name:Monash University | |||||||||||||||||||||||
Full Title: 20% Albumin infusion and AKI following cardiac surgery – Randomised Trial | |||||||||||||||||||||||
Medical condition: Acute kidney injury (AKI) is a common complication of cardiac surgery. AKI is defined according to KDIGO criteria in 3 severity stages. KDIGO creatinine-based criteria for diagnosis and staging of... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001701-13 | Sponsor Protocol Number: FFAKI | Start Date*: 2015-09-19 | |||||||||||||||||||||
Sponsor Name:Nordsjællands Hospital. Dept. of Anaesthesiology and Intensive Care. | |||||||||||||||||||||||
Full Title: Forced fluid removal vs. usual care in intensive care patients with high-risk acute kidney injury and severe fluid overload (FFAKI) – A randomized clinical trial | |||||||||||||||||||||||
Medical condition: Fluid overload associated with acute kidney injury in patients admitted to the intensive care unit | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004223-12 | Sponsor Protocol Number: CT-1KIDN-01 | Start Date*: 2012-08-27 | |||||||||||
Sponsor Name:Digna Biotech S.L. | |||||||||||||
Full Title: A pilot, randomised, double blind, placebo-controlled, parallel groups, clinical trial to investigate the efficacy and safety of Cardiotrophin-1 (CT-1) in kidney transplantation. | |||||||||||||
Medical condition: Kidney transplantation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002594-28 | Sponsor Protocol Number: APHP200036 | Start Date*: 2022-10-05 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Graft Acute kidney injury: vitamin B3 to facilitate renal Recovery In the Early Life of a transplant | |||||||||||||
Medical condition: Patients with end-stage renal failure treated with extrarenal purification (hemodialysis using a catheter or a fistula, or peritoneal dialysis), registered on the national kidney donation waiting l... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003890-23 | Sponsor Protocol Number: Cisplatin | Start Date*: 2021-02-23 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The nephroprotective effect of short hydration during cisplatin treatment in head and neck cancer patients. | ||
Medical condition: Cisplatin induced nephrotoxicity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000887-23 | Sponsor Protocol Number: CTIN816B12201 | Start Date*: 2022-10-03 | ||||||||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||
Full Title: A multicenter, participant and investigator-blinded, randomized, placebo-controlled Phase 2a study to investigate the pharmacokinetics, pharmacodynamics, safety and tolerability of TIN816 in the tr... | ||||||||||||||||||
Medical condition: Acute kidney injury Due to sepsis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Restarted) FR (Completed) DE (Completed) BE (Completed) HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022630-92 | Sponsor Protocol Number: AP214-CS007 | Start Date*: 2010-11-05 | |||||||||||
Sponsor Name:Action Pharma A/S | |||||||||||||
Full Title: An Explorative Phase 2, Randomized, Double-Blind, Placebo-Controlled, Safety and Efficacy Trial of two Dosing Regimens of AP214 for the Prevention of Kidney Injury in Patients Undergoing Cardiac Su... | |||||||||||||
Medical condition: Action Pharma is developing AP214 Acetate for the prevention of postsurgical kidney injury after cardiac surgery. Trial population is patients with increased risk for development of Kidney Inju... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004040-19 | Sponsor Protocol Number: 21-ROS-05 | Start Date*: 2022-02-09 | |||||||||||
Sponsor Name:Guard Therapeutics International AB | |||||||||||||
Full Title: A Phase 2, Randomized, Placebo-Controlled, Double-Blind, Adaptive, Parallel Group Clinical Study to Evaluate the Efficacy and Safety of RMC-035 in Subjects at High Risk for Acute Kidney Injury Foll... | |||||||||||||
Medical condition: Cardiac surgery associated acute kidney injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002547-29 | Sponsor Protocol Number: ATB-203 | Start Date*: 2019-11-21 | ||||||||||||||||||||||||||
Sponsor Name:Atox Bio | ||||||||||||||||||||||||||||
Full Title: Phase 2 randomized, double-blind, placebo-controlled, parallel-group study to evaluate the safety and efficacy of Reltecimod as compared to placebo in addition to standard of care in patients with ... | ||||||||||||||||||||||||||||
Medical condition: Acute kidney injury due to intra-abdominal infection/sepsis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) BE (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001922-24 | Sponsor Protocol Number: 120541 | Start Date*: 2013-07-12 | |||||||||||
Sponsor Name:University College London (UCL) | |||||||||||||
Full Title: The effect of remote ischaemic preconditioning and glyceryl trinitrate on peri-operative myocardial injury in cardiac bypass surgery patients (ERIC-GTN study)- a four arm randomised controlled trial | |||||||||||||
Medical condition: We are investigating the phenomenon of ischaemic-reperfusion injury. Reperfusion of the ischaemic myocardium is known to cause further myocardial damage. We wish to investigate the phenomenon of Re... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003298-24 | Sponsor Protocol Number: EVITAESTEROIDE-12 | Start Date*: 2014-06-26 | |||||||||||
Sponsor Name:Sociedad Andaluza de Trasplante de Órganos y Tejidos (SATOT) | |||||||||||||
Full Title: Steroid withdrawal and novo donor-specific anti-HLA antibodies in renal transplant patients: a prospective, randomized and controlled study in parallel groups. | |||||||||||||
Medical condition: Kidney transplantaion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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: 2010-020452-64 | Sponsor Protocol Number: version2.0 | Start Date*: 2010-10-05 | |||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | |||||||||||||
Full Title: A prospective randomisd open label study to determine the effects of intravenous iron administration on markers of acute kidney injury in chronic kidney disease (CKD) | |||||||||||||
Medical condition: patients with known chonic kidney disease with functional or absolute Iron deficiency Anaemia, and are greater than 18 years will be given repleacement iron therapy accoring to current local protoc... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2012-000756-34 | Sponsor Protocol Number: 2012.001 | Start Date*: 2012-11-02 |
Sponsor Name:NeuroVive Pharmaceutical AB | ||
Full Title: Copenhagen Head Injury Ciclosporin (CHIC) Study: An open-label, uncontrolled Phase II -study to investigate pharmacokinetics, safety and biomarkers of effectiveness of NeuroSTAT® (ciclosporin) i... | ||
Medical condition: Severe Traumatic Brain Injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-004625-24 | Sponsor Protocol Number: AP-recAP-AKI-03-01 | Start Date*: 2020-09-04 | |||||||||||||||||||||
Sponsor Name:AM-Pharma B.V. | |||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Two-Arm Parallel Group, Multi-Center Phase 3 Pivotal Trial to Investigate the Efficacy and Safety of Recombinant Human Alkaline Phosphatase for Treat... | |||||||||||||||||||||||
Medical condition: Sepsis-associated acute kidney injury | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Prematurely Ended) NL (Completed) DK (Prematurely Ended) FI (Completed) DE (Prematurely Ended) GB (GB - no longer in EU/EEA) BE (Completed) IE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001322-54 | Sponsor Protocol Number: CS/2018/6632 | Start Date*: 2020-06-15 | ||||||||||||||||||||||||||
Sponsor Name:University Hospitals Bristol and Weston NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: Carbon Dioxide Insufflation and Brain Protection During Open Heart Surgery: A Randomised Controlled Trial | ||||||||||||||||||||||||||||
Medical condition: Brain injury during open heart valve surgery | ||||||||||||||||||||||||||||
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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: 2017-001604-30 | Sponsor Protocol Number: 1001 | Start Date*: 2017-12-11 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Safety, Tolerability and Efficacy of anti-IL-6 Antibody Clazakizumab in Late Antibody-Mediated Rejection after Kidney Transplantation - A Pilot Trial | ||
Medical condition: Antibody-mediated rejection of a kidney transplant | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004555-79 | Sponsor Protocol Number: 16-115 | Start Date*: 2017-08-08 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: Impact of preoperative midazolam on outcome of elderly patients: a multicenter randomised controlled trial | ||
Medical condition: Under investigation are elderly patients (≥65 years of age) undergoing each kind of surgery with planned general or combined regional and general anaesthesia. Primary, we will investigate the posto... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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) |
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