- Trials with a EudraCT protocol (53)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
53 result(s) found.
Displaying page 1 of 3.
| EudraCT Number: 2012-004758-27 | Sponsor Protocol Number: V1 | Start Date*: 2013-01-30 |
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Augenheilkunde | ||
| Full Title: fMRI analysis of the visual cortex in neovascular age-related macular degeneration | ||
| Medical condition: 20 patients with neovascular age-related macular degeneration will be examined before and after 3 monthly administered intravitreal ranibizumab injections according to the label with 7 tesla magnet... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-003586-45 | Sponsor Protocol Number: Painscales_Sedation_1 | Start Date*: 2009-09-24 |
| Sponsor Name:Department of Anaesthesie, General Intensive Care and Pain Therapy | ||
| Full Title: The precision of three pain scales as a function of sedation | ||
| Medical condition: This is a patient study in patients with a planned operation under general anaesthesie including healthy or merately ill patients (anaesthesia risk classification ASA 1-3). Pain self assessment as ... | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003117-25 | Sponsor Protocol Number: V3.0 | Start Date*: 2018-05-17 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Longitudinal chemodenervation effects of botulinum toxin A after intramuscular application and the impact of physical activity | ||
| Medical condition: Spastic hemiparesis with involvement of the M. biceps brachii | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003184-65 | Sponsor Protocol Number: TPL107 | Start Date*: 2020-02-24 |
| Sponsor Name:Vifor Pharma | ||
| Full Title: POREIIL - Postoperative replacement of intraoperative iron losses | ||
| Medical condition: perioperative bleeding induced iron losses and anemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001730-19 | Sponsor Protocol Number: v1-2 | Start Date*: 2022-02-24 |
| Sponsor Name:Medical Univerity of Vienna | ||
| Full Title: Hormones and Muscle – Unravelling the metabolic pathways of endocrine myopathies A translational magnetic resonance spectroscopy and imaging pilot study | ||
| Medical condition: Hypothyroidism Hypoparathyroidism | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004889-18 | Sponsor Protocol Number: 1.3 | Start Date*: 2022-04-21 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Effect of Dupilumab in patients with aspirin-exacerbated respiratory disease (AERD) -A single-center prospective pilot study | ||
| Medical condition: Aspirin-exacerbated respiratory disease (AERD), also known as Samter's Triad or Widal's triad, comprises the triad of allergic asthma, chronic rhinosinusitis with nasal polyps (CRswNP) and nonstero... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-000043-74 | Sponsor Protocol Number: PNAS0122 | Start Date*: 2023-07-27 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Defining and predicting neonatal inadaptation after gestational exposure to antidepressants: longitudinal exploratory analysis of psychoneuroendocrine risk factors and complications | ||
| Medical condition: major depressive disorder poor neonatal adaptation syndrome (after antidepressant use during pregnancy) | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-003825-24 | Sponsor Protocol Number: 2059/2022 | Start Date*: 2024-03-15 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Drug Concentration and degradation profiles of steroid and antibiotic eye drops in human aqueous humor. | ||
| Medical condition: Postoperative inflammatory response - pharmakokinetics of steroids and antibiotics applied as eye drops | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Ongoing) | ||
| Trial results: (No results available) | ||
| 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: 2006-001910-33 | Sponsor Protocol Number: AGAL02603 | Start Date*: 2007-12-05 | |||||||||||
| Sponsor Name:Genzyme Europe BV | |||||||||||||
| Full Title: A Multicenter, Multinational Study of the Effects of Fabrazyme® (agalsidase beta) Treatment on Lactation and Infants | |||||||||||||
| Medical condition: Fabry disease | |||||||||||||
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| Population Age: In utero, Newborns, Infants and toddlers, Children, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) AT (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004464-57 | Sponsor Protocol Number: SWIFT-DIRECT | Start Date*: 2019-04-17 |
| Sponsor Name:Universtiy Hospital Bern | ||
| Full Title: Solitaire™ With the Intention For Thrombectomy Plus Intravenous t-PA Versus DIRECT Solitaire™ Stent-retriever Thrombectomy in Acute Anterior Circulation Stroke | ||
| Medical condition: Acute Anterior Circulation Stroke | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) ES (Ongoing) AT (Completed) GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002103-33 | Sponsor Protocol Number: 1080719 | Start Date*: 2019-02-26 | |||||||||||
| Sponsor Name: AZ Sint-Jan Brugge-Oostende AV | |||||||||||||
| Full Title: Pulmonary vein isolation with versus without continued antiarrhythmic drug treatment in subjects with persistent atrial fibrillation: a prospective multi-centre randomized controlled clinical study... | |||||||||||||
| Medical condition: Symptomatic persistent atrial fibrillation: atrial fibrillation, that lasts longer than 7 days, including episodes that are terminated by cardioversion, either with drugs or by direct current cardi... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) DK (Completed) ES (Ongoing) FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005450-30 | Sponsor Protocol Number: ABI-MS-P01 | Start Date*: 2014-01-08 |
| Sponsor Name:Medizinische Universität Innsbruck | ||
| Full Title: Anti-Biopharmaceutical Immunization: Prediction and analysis of clinical relevance to minimize the risk of immunization in multiple sclerosis patients on interferon-beta treatment | ||
| Medical condition: Development of neutralising antibodies against Interferon-beta in the treatment of multiple sclerosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-001776-21 | Sponsor Protocol Number: NCT00687882 | Start Date*: 2016-03-10 |
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für | ||
| Full Title: Prospective Multi-Center Evaluation of the Duration of Therapy for Thrombosis in Children | ||
| Medical condition: Thrombosis in pediatric patients | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: AT (Completed) NL (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002643-18 | Sponsor Protocol Number: REDUCE | Start Date*: 2018-09-04 | |||||||||||||||||||||
| Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||||||||||||
| Full Title: REDUCE - Multicenter, prospective, randomized study investigating the efficacy and safety of a reduced immunosuppressive therapy with tacrolimus once daily in comparison to standard triple immunosu... | |||||||||||||||||||||||
| Medical condition: Immunosuppression after kidney transplantion in elderly patients ≥65 years of age | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Ongoing) GB (GB - no longer in EU/EEA) AT (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-005933-34 | Sponsor Protocol Number: SFHI01 | Start Date*: 2021-08-09 | |||||||||||
| Sponsor Name:Sorin CRM SAS (Microport CRM) | |||||||||||||
| Full Title: Evaluation of a modified Anti-Platelet Therapy associated with low-dose rapamycin DES Firehawk in Acute Myocardial Infarction Patients treated with complete revascularization strategy | |||||||||||||
| Medical condition: Patients with clinically stable, low to moderate complexity acute Myocardial Infarction (MI; troponine-positive Non-ST-Elevation MI or ST-Elevation MI) requiring primary Percutaneous Coronary Inte... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) NL (Trial now transitioned) ES (Ongoing) IT (Ongoing) PT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000239-34 | Sponsor Protocol Number: PONTIACII | Start Date*: 2015-12-30 |
| Sponsor Name:Medizinische Universität Wien | ||
| Full Title: NT-proBNP Selected PreventiOn of cardiac eveNts in a populaTion of dIabetic patients without A history of Cardiac disease; a prospective randomized trial | ||
| Medical condition: The purpose of this study is to evaluate the effect of high dose Renin-Angiotensin System (RAS)-antagonists and beta-blocker treatment for the primary prevention of cardiac events in a population o... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) NL (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) HU (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001485-41 | Sponsor Protocol Number: AMAD001 | Start Date*: 2005-04-20 |
| Sponsor Name:Institute for Neurodegenerative Disorders | ||
| Full Title: A single-blinded assessment of the short-term effects of cabergoline vs. carbidopa/levodopa on SPECT dopamine transporter density in out-patient subjects with Parkinson’s Disease | ||
| Medical condition: Approximately 120 recently diagnosed/early Parkinson’s disease subjects, who are untreated (see exclusionary criteria). | ||
| Disease: | ||
| Population Age: | Gender: Male, Female | |
| Trial protocol: AT (Completed) GB (Prematurely Ended) ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005106-23 | Sponsor Protocol Number: ALLSCT06BFMi | Start Date*: 2007-06-27 | |||||||||||
| Sponsor Name:St. Anna Kinderkrebsforschung | |||||||||||||
| Full Title: Allogenic stem cell transplantation in children and adolescents with acute lymphoblastic leukaemia | |||||||||||||
| Medical condition: very high risk acute lymphoblastic leukaemia in children and adolescents with indicaton for allogenic hematopoetic stem cell transplantation | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) IT (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002748-10 | Sponsor Protocol Number: CC-10004-PSA-014 | Start Date*: 2019-02-26 | |||||||||||
| Sponsor Name:Amgen Inc. | |||||||||||||
| Full Title: A Phase 4, Multicenter, Single-Arm, Open-Label Study to Evaluate the Impact of Apremilast (CC-10004) on MRI Outcomes in Subjects with Psoriatic Arthritis | |||||||||||||
| Medical condition: Psoriatic arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) AT (Completed) DK (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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