- Trials with a EudraCT protocol (14,202)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14,202 result(s) found for: Blood Test.
Displaying page 168 of 711.
EudraCT Number: 2010-024225-20 | Sponsor Protocol Number: 301110_PALANCE | Start Date*: 2014-08-22 |
Sponsor Name:University Hospital Munich, Germany | ||
Full Title: The impact of phosphate balanced cristalloid infusion on acid-base homeostastis | ||
Medical condition: This study aims to investigate a new crystalloid fluid therapy regime for the perioperative setting providing stable fluid and acid-base homeostasis in the patient. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005585-32 | Sponsor Protocol Number: 111111733104 | Start Date*: 2016-06-24 | |||||||||||
Sponsor Name:Department of Biomedical Sciences, Faculty of Health Sciences, University of Copenhagen | |||||||||||||
Full Title: Synergy effect of the appetite hormone GLP-1 (LiragluTide) and Exercise on maintenance of weight loss and health after a low calorie diet - the S-LiTE randomized trial | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000024-13 | Sponsor Protocol Number: aspirin v1 | Start Date*: 2006-03-19 |
Sponsor Name:Cardiff and Vale NHS Trust | ||
Full Title: Does Aggressive management with early high dose aspirin reduce the hypercoagulability of platelets following coronary artery bypass grafting? | ||
Medical condition: Aspirin is an antiplatelet drug that affects the ability of platelets in the blood to bind together and form clots. It is used routinely in patients with or at risk of heart disease and after surg... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001202-84 | Sponsor Protocol Number: lithium-15-12-06 | Start Date*: 2007-02-01 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: Comparison of the action of amiloride and thiazide in the reduction of lithium-NDI in patients with affective disorders | |||||||||||||
Medical condition: Lithium-induced Nephrogenic Diabetes Insipidus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006922-32 | Sponsor Protocol Number: HOADO | Start Date*: 2009-02-09 | |||||||||||
Sponsor Name:RUNMC | |||||||||||||
Full Title: Heme oxygenase (HO) activity in humans. Effects of heme arginate (Normosang®) on parameters of HO activity and on adenosine induced vasodilation. | |||||||||||||
Medical condition: Normosang treatment will be used to evaluate heme oxygenase induction in healthy subjects. Results will be used for future studies concerning diabetes related cardiovascular disease. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001340-19 | Sponsor Protocol Number: NLROW.1012.15 | Start Date*: 2016-07-21 |
Sponsor Name:Radboud University Medical Center | ||
Full Title: An uncontrolled, pilot-study assessing the efficacy of octreotide LAR to decrease transfusion requirements and endoscopy frequency in patients with Rendu-Osler-Weber and gastrointestinal bleeding | ||
Medical condition: Patients with Rendu-Osler-Weber disease (which is also called: Hereditary hemorrhagic telangiectasia) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004758-33 | Sponsor Protocol Number: Rapid-study | Start Date*: 2015-09-08 | |||||||||||
Sponsor Name:Medical University of Vienna | |||||||||||||
Full Title: Randomized Assessment of patients with clinically suspected Prostate cancer after multiparametric metabolic hybrid Imaging to evaluate its potential clinical Domain: A prospective, randomized, mult... | |||||||||||||
Medical condition: Clinical suspected prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002470-42 | Sponsor Protocol Number: FluSHED-2 | Start Date*: 2018-08-30 | |||||||||||
Sponsor Name:Imperial College London JRC Office | |||||||||||||
Full Title: Assessment of viral shedding week following administration of live attenuated influenza vaccine in children: FluSHED-2 study | |||||||||||||
Medical condition: Prevention of influenza infection through immunisation | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005595-35 | Sponsor Protocol Number: CHDR2036 | Start Date*: 2021-02-11 | |||||||||||
Sponsor Name:Centre for Human Drug Research | |||||||||||||
Full Title: A dermal inflammatory challenge study to evaluate complement activation in healthy volunteers | |||||||||||||
Medical condition: Inflammation / Complement activation | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001375-32 | Sponsor Protocol Number: PreToVid | Start Date*: 2020-04-03 |
Sponsor Name:UMCG | ||
Full Title: Pre-emptive tocilizumab in hypoxic COVID-19 patients, a prospective randomized trial | ||
Medical condition: Hypoxia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-024625-20 | Sponsor Protocol Number: LUMC2010-02 | Start Date*: 2012-05-22 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: ADMINISTRATION OF HA-1 TCR TRANSDUCED VIRUS-SPECIFIC T-CELLS AFTER ALLOGENEIC STEM CELL TRANSPLANTATION IN PATIENTS WITH HIGH-RISK LEUKEMIA (LUMC 2010-02) | ||
Medical condition: high risk leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-001958-10 | Sponsor Protocol Number: IMUNOR-201301 | Start Date*: 2013-09-04 | |||||||||||
Sponsor Name:ImunomedicA, a.s. | |||||||||||||
Full Title: A Prospective, Randomized, Double-Blind, Placebo-controlled, Multicenter, Phase III Confirmatory Study Assessing Efficacy and Safety of the IMUNOR Therapy Versus Placebo in Children with Recurrent ... | |||||||||||||
Medical condition: Recurrent Respiratory Tract Infections | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003430-25 | Sponsor Protocol Number: 101HEMB02 | Start Date*: 2017-05-18 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceutical, Inc. | |||||||||||||
Full Title: A Long-Term Follow-up Study to Evaluate the Safety, Tolerability, and Efficacy of Adeno-Associated Virus (AAV) rh10-Mediated Gene Transfer of Human Factor IX in Adults With Moderate/Severe to Sever... | |||||||||||||
Medical condition: Moderate/severe to severe hemophilia B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002934-34 | Sponsor Protocol Number: 2020-AKA | Start Date*: 2020-11-04 | |||||||||||
Sponsor Name:Aarhus University Hospital, dept. of Diabetes and Hormonal diseases | |||||||||||||
Full Title: The effects of melatonin treatment on bone, marrow, sleep and arterial stiffness in postmenopausal women | |||||||||||||
Medical condition: Osteoporosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005031-32 | Sponsor Protocol Number: Diabetes2017 | Start Date*: 2017-10-10 | |||||||||||
Sponsor Name:Pirkanmaan sairaanhoitopiiri | |||||||||||||
Full Title: Metformin use to improve pregnancy outcome in women with type 1 diabetes. A double-blind placebo-controlled multicenter study. | |||||||||||||
Medical condition: Pregnancy of a women dealing with type 1 diabetes | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001863-35 | Sponsor Protocol Number: THAM | Start Date*: 2016-06-21 |
Sponsor Name:Universitätsklinik für Klinische Pharmakologie, Medizinische Universität Wien | ||
Full Title: Effects of Tromethamine on Cerebral Oxygenation and Metabolism in Patients Suffering Intractable Intracranial Hypertension – an exploratory study. | ||
Medical condition: Critically ill patients (SAH, ICB, AVM bleedings, malignant MCA infarcts) under sedation and mechanical ventilation in need of multimodality monitoring, including brain tissue oxygen monitoring and... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-001904-12 | Sponsor Protocol Number: 18040 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: Desmopressin for reversal of Antiplatelet drugs in Stroke due to Haemorrhage (DASH) | |||||||||||||
Medical condition: Intracerebral haemorrhage | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003163-21 | Sponsor Protocol Number: COTHUGMTRA22 | Start Date*: 2023-07-13 | |||||||||||
Sponsor Name:Coral Sánchez Pérez | |||||||||||||
Full Title: PHASE III, SINGLE-CENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, LOW-INTERVENTION CLINICAL TRIAL IN TWO PARALLEL GROUPS, TO EVALUATE EFFICACY AND SAFETY IN ELDERLY PATIENTS WITH PERTROCHANTE... | |||||||||||||
Medical condition: pertrochanteric hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000017-20 | Sponsor Protocol Number: ASS-Metamizol-DDI | Start Date*: 2018-07-17 |
Sponsor Name:Universitäts-Herzzentrum Freiburg • Bad Krozingen | ||
Full Title: Antiplatelet effect of acetylsalicylic acid in patients after cardiac surgery: Impact of dipyrone (metamizole) | ||
Medical condition: Antithrombotic therapy after surgical replacement of stenotic heart valve by a bioprosthesis or mitral valve repair | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005068-16 | Sponsor Protocol Number: 221181 | Start Date*: 2018-02-14 | |||||||||||
Sponsor Name:University Hospital of Aarhus | |||||||||||||
Full Title: Measurement of Acetylsalicylic acid Concentration and Effect - MACE | |||||||||||||
Medical condition: Healthy volunteers (Prophylaxis of arterial thrombosis) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
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