- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
67 result(s) found for: Continuous renal replacement therapy.
Displaying page 1 of 4.
EudraCT Number: 2012-005617-39 | Sponsor Protocol Number: WS2030571 | Start Date*: 2014-01-14 |
Sponsor Name:University Hospital Tuebingen | ||
Full Title: Pharmacokinetics of Tigecycline in Patients Receiving Continuous Renal Replacement Therapy | ||
Medical condition: Surgical ICU patients with severe infection and renal replacement therapy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000899-16 | Sponsor Protocol Number: UMM022013TG | Start Date*: 2013-10-16 |
Sponsor Name:Department of Pharmacy Unversitätsmedizin Mainz | ||
Full Title: Investigation of pharmacokinetics of Linezolid and Meropenem in patients receiving continuous renal replacement therapy | ||
Medical condition: Sepsis and acute renal failure (ARF) are pathological entities that commonly co-exist in patients admitted to intensive care. Antibiotic dosing in septic patients with ARF can be complicated and ma... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001019-95 | Sponsor Protocol Number: COLIMICINA | Start Date*: 2021-05-31 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Pharmacokinetic/pharmacodynamic aspects of colistin intravenous administration in critically ill patients suffering from hospital infections caused by multi-antibiotic-resistant germs and receiving... | |||||||||||||
Medical condition: Critically ill patients suffering from hospital infections caused by multi-antibiotic-resistant germs and receiving continuous renal replacement therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021369-66 | Sponsor Protocol Number: UMM062010FS | Start Date*: 2010-11-16 |
Sponsor Name:Department of Pharmacy Universitaetsmedizin Mainz | ||
Full Title: Investigation of pharmacokinetics of Ciprofloxacin and Piperacillin/Tazobactam in Patients receiving continuous renal replacement therapy | ||
Medical condition: Sepsis and acute renal failure (ARF) are two pathological entities that commonly co-exist in patients admitted to intensive care. Antibiotic dosing in septic patients with ARF can be complicated a... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004361-12 | Sponsor Protocol Number: FER-CIT-2016-01 | Start Date*: 2017-03-27 | ||||||||||||||||
Sponsor Name:Fernando Sánchez | ||||||||||||||||||
Full Title: Oxidative stress and extracellular nucleosomes in critically ill patients with acute kidney failure treated with continuous renal replacement therapies. Effect of two anticoagulation strategies of ... | ||||||||||||||||||
Medical condition: Acute renal failure (ARF). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000904-14 | Sponsor Protocol Number: MICA_HDF | Start Date*: 2012-07-19 | |||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||
Full Title: PHARMACOKINETICS OF MICAFUNGIN DURING CONTINUOUS VENOVENOUS HEMOFILTRATION | |||||||||||||
Medical condition: Suspected or proven candida infection requiring parenteral antifungal therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023455-28 | Sponsor Protocol Number: 11102010 | Start Date*: 2010-12-15 | |||||||||||
Sponsor Name:Maija Kaukonen | |||||||||||||
Full Title: Dexmedetomidine pharmacokinetics during continuous venovenous hemofiltration and hemodiafiltration in critically ill patients | |||||||||||||
Medical condition: Intensive care patients with acute kidney injury requiring continuous renal replacement therapy with a clinical indication for sedation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004854-33 | Sponsor Protocol Number: 03-AnIt-14/UKM14_0066 | Start Date*: 2016-02-05 | ||||||||||||||||
Sponsor Name:University Hospital Muenster | ||||||||||||||||||
Full Title: Regional citrate versus systemic heparin anticoagulation for continuous renal replacement therapy in critically ill patients with acute kidney injury (RICH-Trial). | ||||||||||||||||||
Medical condition: Critically ill patients with acute kidney injury | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-006789-19 | Sponsor Protocol Number: NephroD_2021 | Start Date*: 2022-05-16 | |||||||||||
Sponsor Name:USK w Opolu | |||||||||||||
Full Title: Efficacy comparison of two doses of vitamin D3 in critically ill patients undergoing continuous renal replacement therapy - NephroD | |||||||||||||
Medical condition: Vitamin D3 deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002069-11 | Sponsor Protocol Number: 1 | Start Date*: 2008-09-10 | ||||||||||||||||
Sponsor Name:Medizinische Universität Wien, Univ. Klinik für Innere Medizin III, Abteilung für Gastroenterologie | ||||||||||||||||||
Full Title: PHARMACOKINETICS OF GANCICLOVIR DURING CONTINUOUS RENAL REPLACEMENT THERAPY | ||||||||||||||||||
Medical condition: Medical Intensive Care Unit Renal failure Renal Replacement Therapy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-003211-69 | Sponsor Protocol Number: LOC 06 / 2004-02 | Start Date*: 2005-09-20 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Anticoagulation with Prostaglandin E1 and unfractioned Heparin versus Placebo and unfractioned Heparin during continuous venovenous hemofiltration | ||
Medical condition: Male and female patients with acute renal failure and treated with continuous venovenous hemofiltration therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003403-29 | Sponsor Protocol Number: TMP-SMT-CVVH | Start Date*: 2014-09-26 |
Sponsor Name:Innsbruck Medical University | ||
Full Title: Pharmacokinetics of trimethoprim-sulfametrole in critically ill patients on continuous veno-venous haemofiltration | ||
Medical condition: Life-threatening infection treated with trimethoprim-sulfametrole (Rokiprim) in critically ill patients on and off continuous veno-venous haemfiltration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004106-87 | Sponsor Protocol Number: CAS CVVH | Start Date*: 2007-10-23 |
Sponsor Name:Meical University, Dpt. Internal Medicine, Div. of General Internal Medicine | ||
Full Title: CLINICAL PHARMACOKINETICS OF CASPOFUNGIN IN CRITICALLY ILL PATIENTS DURING CONTINUOUS VENO-VENOUS HEMOFILTRATION | ||
Medical condition: Plasma concentrations of Caspofungin will be measured in patients requiring treatment with Cancidas (Caspofungin) and continuous veno-venous hemofiltration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002077-12 | Sponsor Protocol Number: MR-2008/001 | Start Date*: 2008-09-24 | |||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PERUGIA | |||||||||||||||||||||||
Full Title: Fenoldopam end Renal failure (FENO-HSR) | |||||||||||||||||||||||
Medical condition: Renal failure from ipoperfusion post Cardiac surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003914-42 | Sponsor Protocol Number: CEFTAROLINE_RRT | Start Date*: 2013-11-06 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Univ.-Klinik für Innere Medizin I, Klinische Abteilung für Infetionen und Tropenmedizin | |||||||||||||
Full Title: Multiple-dose Pharmacokinetics of Ceftaroline during continuous and intermittent renal replacement therapy in patients requiring renal replacement therapy | |||||||||||||
Medical condition: Bacterial infection in patients recieving renal replacement therapy | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001391-15 | Sponsor Protocol Number: V323Oct2020 | Start Date*: 2020-04-24 | |||||||||||
Sponsor Name:Royal College of Surgeons Ireland | |||||||||||||
Full Title: A randomized double-blind placebo-controlled, pilot trial of intravenous plasma-purified alpha-1 antitrypsin for severe COVID-19 illness. | |||||||||||||
Medical condition: acute respiratory distress sydnrome (ARDS) secondary to Covid-19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003798-82 | Sponsor Protocol Number: R1578 | Start Date*: 2014-01-29 | |||||||||||
Sponsor Name:Hull & East Yorkshire Hospitals NHS Trust | |||||||||||||
Full Title: Multi-centre Randomised Controlled Trial of Angiotensin Converting Enzyme inhibitor (ACEi) / Angiotensin Receptor Blocker (ARB) withdrawal in advanced renal disease; The STOP-ACEi Trial | |||||||||||||
Medical condition: Progressive, advanced (stage 4 or 5) chronic kidney disease (CKD). NB. There was not an appropriate therapeutic area in the drop down menu in E1-1. Have selected 'Male diseases of the urinary and... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007753-12 | Sponsor Protocol Number: 1.0 | Start Date*: 2010-01-21 | |||||||||||
Sponsor Name:MUW, Universitätsklinik für Innere Medizin I, Abteilung für Infektionskrankheiten und Tropenmedizin | |||||||||||||
Full Title: The pharmacokinetics of anidulafungin during continuous venovenous hemofiltration | |||||||||||||
Medical condition: intensive care patients with suspected or proven fungal infection, who undergo hemofiltration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000291-19 | Sponsor Protocol Number: COL-ECMO2022 | Start Date*: 2022-06-21 |
Sponsor Name:Fakultní nemocnice u sv. Anny v Brně | ||
Full Title: Pharmacokinetics of colistin in critically ill patients with extracorporeal membrane oxygenation | ||
Medical condition: Pharmacokinetics in critically ill | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004426-24 | Sponsor Protocol Number: 951/07 | Start Date*: 2007-07-06 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: PROSTACYCLIJN VERSUS HEPARIN AS ANTICOAGULANT IN CONTINUOUS VENO-VENOUS HEMODIAFILTRATION | |||||||||||||
Medical condition: Acute renale failure in intensive unit | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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