- Trials with a EudraCT protocol (348)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
348 result(s) found for: Human albumin.
Displaying page 1 of 18.
| EudraCT Number: 2016-004012-35 | Sponsor Protocol Number: ALB-INFUS | Start Date*: 2017-01-13 |
| Sponsor Name:Medical University of Graz | ||
| Full Title: Effect of albumin infusion on oxidative albumin modification, albumin binding capacity and plasma thiol status | ||
| Medical condition: refractory ascites, spontaneous bacterial peritonitis, hepatorenal syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-000996-26 | Sponsor Protocol Number: VAB1 | Start Date*: 2016-09-01 |
| Sponsor Name:Region Ostergotland | ||
| Full Title: Volumekinetics for hyperoncotic albumin in burn patients as well as for healthy subjects. | ||
| Medical condition: Healthy adult volunteers and burn patients 3 to 10 Days after the injury. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| 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: 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: 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: 2005-005083-81 | Sponsor Protocol Number: ALBUCARD | Start Date*: 2006-06-09 |
| Sponsor Name:HOSPITAL CLINIC | ||
| Full Title: EFECTOS DE LA ADMINISTRACIÓN DE ALBÚMINA INTRAVENOSA SOBRE LA FUNCIÓN DIASTÓLICA DE LOS PACIENTES CON CIRROSIS HEPÁTICA. | ||
| Medical condition: Liver cirrhosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003687-12 | Sponsor Protocol Number: RAV1.2 | Start Date*: 2017-11-22 |
| Sponsor Name:Region Ostergotland | ||
| Full Title: Infusion rate and volumekinetics for hyperoncotic albumin in healthy subjects (RAV), - A phase IV, randomized, open-labeled, cross-over study | ||
| Medical condition: Healthy adult volunteers Fluid mobilisation. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003027-30 | Sponsor Protocol Number: IIBSP-ALB-2017-72 | Start Date*: 2017-11-27 |
| Sponsor Name:Institut de Recerca Hospital de la Santa Creu i Sant Pau | ||
| Full Title: Influence of albumin on the development of acute renal dysfunction associated with cardiac surgery under extracorporeal circulation | ||
| Medical condition: Renal function | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| 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: 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: 2016-001940-20 | Sponsor Protocol Number: | Start Date*: 2016-10-11 | |||||||||||
| Sponsor Name:Central Manchester University Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: A Pilot, Randomised, Unblinded, Feasibility, Safety, Biochemical and Physiological Efficacy Study of 20% vs 5% Human Albumin Solution for Fluid Bolus Therapy in Critically Ill Adults | |||||||||||||
| Medical condition: Hypovolaemia associated with critical illness | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001135-20 | Sponsor Protocol Number: Albumin | Start Date*: 2015-04-28 |
| Sponsor Name:Södertälje sjukhus AB | ||
| Full Title: Volume kinetics for 20% albumin in conscious and anaesthetized humans with and without inflammation. | ||
| Medical condition: Healthy adult volunteers, healthy patients undergoing surgery under general anesthesia, and patients in a state of inflammation after having undergone surgery under general anaesthesia (within 24 h... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019783-37 | Sponsor Protocol Number: MZ10-NETR-RadvanMartin | Start Date*: 2010-06-15 |
| Sponsor Name:Hospital Trebic | ||
| Full Title: Two doses of albumin after large paracentesis in cirrhotics with refractory ascites: a randomized study | ||
| Medical condition: patients with decompensated liver cirrhosis and refractery ascites indicated for large /more then 5 L/ volume paracentesis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| 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: 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: 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: 2021-000861-34 | Sponsor Protocol Number: 2021-000861-34 | Start Date*: 2022-07-01 |
| Sponsor Name:Region Ostergotland | ||
| Full Title: Comparison of albumin and Ringer´s solution for optimization of the plasma volume and hemodynamics during surgery. | ||
| Medical condition: Patients in need of major laparoscopic surgery in the abdomen, lasting longer than 90 minutes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002216-14 | Sponsor Protocol Number: 1277 | Start Date*: 2017-07-26 |
| Sponsor Name:Clinical Pharmacology, MUV | ||
| Full Title: Investigation of Pharmacokinetic of Antiinfective Therapy in Healthy Subjects and Severely Burned Patients Admitted to the ICU | ||
| Medical condition: This is an exploratory pharmacokinetic trial in healthy volunteers (cohort A) and patients with severe burns admitted to the ICU (cohort B). The Information retrieved by these investigations will h... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| 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: 2016-001313-24 | Sponsor Protocol Number: SUPERADD | Start Date*: 2017-02-13 | ||||||||||||||||||||||||||
| Sponsor Name:Technische Universität München, Fakultät für Medizin | ||||||||||||||||||||||||||||
| Full Title: SUbstition of PERioperative Albumin Deficiency Disorders | ||||||||||||||||||||||||||||
| Medical condition: High risk surgical patients or procedures showing a hypoalbuminemia intraoperatively. | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
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