- Trials with a EudraCT protocol (1,157)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
1,157 result(s) found for: Serum albumin.
Displaying page 1 of 58.
EudraCT Number: 2007-003769-41 | Sponsor Protocol Number: ALB1 | Start Date*: 2008-01-31 | |||||||||||
Sponsor Name:Medical University Graz | |||||||||||||
Full Title: Albumin in acute-on-chronic liver failure: More than just volume? A randomized, controlled study | |||||||||||||
Medical condition: Spntaneous bacterial peritonitis | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2018-001874-89 | Sponsor Protocol Number: ZKSJ0112_ARISS | Start Date*: 2019-02-25 | ||||||||||||||||
Sponsor Name:Friedrich-Schiller-Universität Jena | ||||||||||||||||||
Full Title: Randomised controlled multicentre study of albumin replacement therapy in septic shock | ||||||||||||||||||
Medical condition: Septic Shock | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002638-35 | Sponsor Protocol Number: 3.00 | Start Date*: 2012-07-31 |
Sponsor Name:Stockholms Läns Landsting, Karolinska Universitetssjukhuset Huddinge, Anestesikliniken | ||
Full Title: ALBUMIN KINETICS BY 123I-HSA A validation study on healthy volunteers, patients with acute inflammation, and patiens scheduled for major abdominal surgery | ||
Medical condition: A) healthy volunteers (transcapillary escape rate of albumin, plasmavolume, and turnover of albumin) B) Acute inflammation such as pancreatitis or cholecystitis C) Scheduled major abdominal surge... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000302-29 | Sponsor Protocol Number: AlbuCAT | Start Date*: 2019-07-31 | |||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | |||||||||||||
Full Title: ALBUMIN FOR MANAGEMENT OF HYPERVOLEMIC HYPONATREMIA IN PATIENTS WITH DECOMPENSATED CIRRHOSIS. A PROOF OF CONCEPT STUDY | |||||||||||||
Medical condition: HYPERVOLEMIC HYPONATREMIA IN PATIENTS WITH DECOMPENSATED CIRRHOSIS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002300-24 | Sponsor Protocol Number: 6.0 | Start Date*: 2015-03-20 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Albumin To prevenT Infection in chronic liveR failurE (ATTIRE) | |||||||||||||
Medical condition: Liver cirrhosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003174-50 | Sponsor Protocol Number: ALBUCEF | Start Date*: 2021-01-28 |
Sponsor Name:Medical University of Vienna Department of Cardiac Thoracic Vascular Anesthesia and Intensive Care Medicine | ||
Full Title: The Effect of Albumin Levels on Pharmacokinetics of Cefazolin in Adult Cardiac Surgery: A Prospective, Randomized, Open-label, Parallel-group Pharmacokinetic Study | ||
Medical condition: effect of hypoalbuminemia on pharmacokinetics of cefazolin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002756-21 | Sponsor Protocol Number: 1663/2020 | Start Date*: 2021-02-23 |
Sponsor Name:Department of Cardiothoracic Anesthesia and Intensive Care Medicine, Medical University of Vienna | ||
Full Title: Plasma Pharmacokinetics of Prophylactic Cefazolin Administered for Cardiac Surgery: Comparison of Cardiopulmonary Bypass Priming with Additive Human Albumin 20% vs.Pure Crystalloid Priming: A singl... | ||
Medical condition: This is a pharmacokinetic trial for patients undergoing cardiac surgery. It will be investigated whether cardiopulmonary bypass priming substituted with human albumin 20% has an effect on the pharm... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002416-27 | Sponsor Protocol Number: INFECIR2 | Start Date*: 2013-10-23 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Fundacio Clinic per a la recerca biomedica | ||||||||||||||||||||||||||||||||||||||
Full Title: Albumin administration in the prevention of hepatorenal syndrome and death in patients with cirrhosis, bacterial infections other than spontaneous bacterial peritonitis and high risk of hospital mo... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with advanced cirrhosis (serum creatinine > 1.2 mg/dl, serum sodium < 130 mEq/l and/or serum bilirubin > 4 mg/dl), signs of systemic inflammation and urinary infection, pneumonia, skin/sof... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NO (Completed) ES (Ongoing) IT (Prematurely Ended) BE (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) DK (Prematurely Ended) IE (Prematurely Ended) GB (Prematurely Ended) NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001949-20 | Sponsor Protocol Number: 1.0 | Start Date*: 2023-01-09 | |||||||||||
Sponsor Name:ALBIMMUNE S.L. | |||||||||||||
Full Title: Human albumin treatment in adult septic shock. A phase 2, multicenter, randomized, controlled study evaluating the immune response and organ failure. | |||||||||||||
Medical condition: Septic Shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003048-37 | Sponsor Protocol Number: HSJC-CAR-01-2015 | Start Date*: 2015-11-13 |
Sponsor Name:Juan Luis Bonilla Palomas | ||
Full Title: Effect of ?-3 polyunsaturated fatty acids on serum albumin concentration in patients with acute heart failure, hypoalbuminemia, and high inflammatory activity | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003825-56 | Sponsor Protocol Number: SENTINELSEEK-HC | Start Date*: 2020-02-28 |
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||
Full Title: An exploratory prospective, open-label, unicentric study with cross-over design, comparing Lymphoseek® vs. albumin nanocolloid for Image-Guided Sentinel Lymph Node Mapping in Head and Neck, Melanom... | ||
Medical condition: The hypothesis is that 99mTc-tilmanocept (Lymphoseek®) can be used safely and will be comparable to nanocolloidal human serum nanocolloidal albumin in Head and Neck, Melanoma and Breast Cancer sent... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003117-18 | Sponsor Protocol Number: HUB-INF-ALBUCAP-402 | Start Date*: 2019-07-10 | |||||||||||
Sponsor Name:Dr. Jordi Carratalà Fernández (Servicio de Enfermedades Infecciosas) del Hospital Universitario de Bellvitge | |||||||||||||
Full Title: A phase III randomized, controlled, open label multicenter clinical trial, with two parallel groups, to evaluate the efficacy of albumin administration in patients hospitalized with community-acqui... | |||||||||||||
Medical condition: Community-acquired pneumonia (CAP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005350-29 | Sponsor Protocol Number: 2013-03-612 | Start Date*: 2014-02-14 | |||||||||||
Sponsor Name:Rigshospitalet [...] | |||||||||||||
Full Title: Effect of Human Albumin versus crystalloid on coagulation competence during elective urologic surgery. | |||||||||||||
Medical condition: Coagulation and loss of blood | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000799-15 | Sponsor Protocol Number: 04-04074 | Start Date*: 2004-09-09 |
Sponsor Name:Aker University Hospital | ||
Full Title: DOES BENFOTIAMINE SUPPLEMENTATION REDUCE SERUM LEVELS OF ADVANCED GLYCATION END PRODUCTS AND BIOCHEMICAL MARKERS OF VASCULAR DYSFUNCTION IN TYPE 1 DIABETES? | ||
Medical condition: Type 1 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000308-82 | Sponsor Protocol Number: oxalate01 | Start Date*: 2017-02-08 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Lanthanum Carbonate (Fosrenol®) to reduce oxalate excretion in patients with secondary hyperoxaluria and nephrolithiasis: a short-term, prospective, open-label, efficacy and safety clinical trial | ||
Medical condition: Urolithiasis and secondary hyperoxaluria | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004809-33 | Sponsor Protocol Number: BETA | Start Date*: 2015-03-09 | ||||||||||||||||
Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) | ||||||||||||||||||
Full Title: Albumin infusion effects in patients with cirrhosis hepatic encephalopathy | ||||||||||||||||||
Medical condition: hepatic encephalopathty | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006749-18 | Sponsor Protocol Number: HE06-001-C P4 | Start Date*: 2009-06-26 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: Efficacy and safety of 6 % hydroxyethyl starch 130/0.4 (Voluven®) vs. 5% HSA in volume replacement therapy during elective open-heart surgery in paediatric patients | |||||||||||||
Medical condition: Volume replacement therapy during elective open-heart surgery in paediatric patients | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005416-26 | Sponsor Protocol Number: ANSWER | Start Date*: 2014-06-06 |
Sponsor Name:Mario Negri Institute | ||
Full Title: A Prospective, Randomized, Open, Blinded Endpoint (PROBE), Clinical Trial to Assess The Renal and Humoral Effects of Sevelamer Carbonate in Patients with Chronic Kidney Disease and Residual Protein... | ||
Medical condition: Chronic Kidney Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004611-50 | Sponsor Protocol Number: CCTU0228 | Start Date*: 2019-06-14 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||
Full Title: A randomised, two-arm (1:1 ratio), double blind, placebo controlled phase III trial to assess the efficacy, safety, cost and cost-effectiveness of rituximab in treating de novo or relapsing NS in p... | ||
Medical condition: Minimal Change Disease (MCD) and Focal segmental glomerulosclerosis (FSGS) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001789-28 | Sponsor Protocol Number: IG1601 | Start Date*: 2018-04-25 | |||||||||||
Sponsor Name:Instituto Grifols S.A. | |||||||||||||
Full Title: Prevention of Mortality with Long-Term Administration of Human Albumin in Subjects with Decompensated Cirrhosis and Ascites | |||||||||||||
Medical condition: Subjects with decompensated cirrhosis and ascites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) FR (Completed) BE (Completed) GB (GB - no longer in EU/EEA) DK (Completed) IT (Completed) HU (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
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