- Trials with a EudraCT protocol (44,347)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,347 result(s) found.
Displaying page 1,232 of 2,218.
EudraCT Number: 2011-004621-26 | Sponsor Protocol Number: Devitahep | Start Date*: 2012-07-31 | |||||||||||||||||||||
Sponsor Name:Medical University Graz | |||||||||||||||||||||||
Full Title: The effect of vitamin D supplementation on immune response following hepatitis B vaccine in incident and prevalent hemodialysis patients with vitamin D deficiency | |||||||||||||||||||||||
Medical condition: The effect of vitamin D supplementation on immune response following hepatitis B vaccine in incident and prevalent hemodialysis patients with vitamin D deficiency | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-009998-10 | Sponsor Protocol Number: MYCUV-IIT02 | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:Centre for Ophthalmology, University of Tuebingen | |||||||||||||
Full Title: Myfortic (enteric-coated mycophenolate sodium) for the treatment of non-infectous intermediate uveitis – a prospective, controlled randomized multicenter trial | |||||||||||||
Medical condition: non-infectious uveitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002897-31 | Sponsor Protocol Number: 1453 | Start Date*: 2006-04-04 |
Sponsor Name:North Bristol NHS Trust | ||
Full Title: Objective assessment of attention difficulties in adults with Attention-Deficit Hyperactivity Disorder (ADHD) | ||
Medical condition: Attention-Deficit Hyperactivity Disorder (ADHD) in Adults | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004210-10 | Sponsor Protocol Number: ASSTBS-BLADE-2540-2016 | Start Date*: 2017-03-29 | ||||||||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||
Full Title: A PILOT PHASE IV STUDY TO EVALUATE VARIATION IN BONE MINERAL DENSITY, LEAN AND FAT BODY MASS MEASURED BY DUAL-ENERGY X-RAY ABSORPTIOMETRY IN PATIENTS WITH PROSTATE CANCER WITHOUT BONE METASTASIS T... | ||||||||||||||||||
Medical condition: prostate cancer prostate cancer without bone metastases | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019140-39 | Sponsor Protocol Number: CPP-450 | Start Date*: 2010-09-06 | ||||||||||||||||||||||||||
Sponsor Name:Centre Paul Papin | ||||||||||||||||||||||||||||
Full Title: Intérêt d'un traitement par cyclines dans la prévention de la toxicité cutanée du Cétuximab lors de son association à un FOLFIRI intensifié chez des patients avec un cancer colorectal en première o... | ||||||||||||||||||||||||||||
Medical condition: Patients atteints d'un cancer colorectal en première ou deuxième ligne métastatique, KRAS sauvages, devant recevoir une chimiothérapie par FOLFIRI intensifié et Cetuximab. le Cetuximab étant à l'or... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002641-11 | Sponsor Protocol Number: PRIDE | Start Date*: 2018-11-21 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: The BRIDGE-PMR study: B-cell depletion with Rituximab for Dose reduction of Glucocorticoids: Efficacy in PolyMyalgia Rheumatica | ||
Medical condition: polymyalgia rheumatica | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000391-42 | Sponsor Protocol Number: MD-01 | Start Date*: 2013-01-22 |
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | ||
Full Title: Investigation on the peritoneal tissue concentrations of antibiotics in surgical patients with peritonitis using microdialysis. Example: linezolide, tigecycline | ||
Medical condition: Peritonitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004657-40 | Sponsor Protocol Number: CTPA-2015 | Start Date*: 2016-06-14 |
Sponsor Name:Region Örebro län | ||
Full Title: Minimizing contrast agent in computed tomography pulmonary angiography | ||
Medical condition: Computed tomography of suspected pulmonary embolism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017823-24 | Sponsor Protocol Number: 1703 | Start Date*: 2010-03-19 |
Sponsor Name:Tartu University Hospital | ||
Full Title: Meropenem pharmacokinetics in very low birth weight neonates | ||
Medical condition: proven or suspected sepsis, lower respiratory tract infection, complicated intraabdominal infection | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: EE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003788-36 | Sponsor Protocol Number: NN7088-4410 | Start Date*: 2018-03-12 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Safety and Efficacy of turoctocog alfa pegol (N8-GP) in Prophylaxis and Treatment of Bleeds in Previously N8-GP Treated Patients with Severe Haemophilia A | |||||||||||||
Medical condition: Haemophilia A | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: LT (Completed) GB (GB - no longer in EU/EEA) PT (Completed) GR (Completed) NO (Completed) DK (Completed) HU (Completed) FR (Completed) NL (Completed) DE (Completed) ES (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005131-40 | Sponsor Protocol Number: MA29957 | Start Date*: 2016-10-20 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE IIb, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY, SAFETY, AND TOLERABILITY OF SILDENAFIL ADDED TO PIRFENIDONE IN PATIENTS WITH ADVANCED IDIOPATH... | |||||||||||||
Medical condition: "Pulmonary Hypertension in patients with Idiopathic pulmonary fibrosis (IPF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) NL (Completed) BE (Completed) DE (Completed) GR (Completed) HU (Completed) CZ (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001152-35 | Sponsor Protocol Number: V114-023 | Start Date*: 2019-05-10 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-blind, Active Comparator-controlled Study to Evaluate the Safety, Tolerability, and Immunogenicity of V114 in Children with Sickle Cell Disease (PNEU–SICKLE) | |||||||||||||
Medical condition: Pneumococcal disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003373-64 | Sponsor Protocol Number: 01-DIMS-2021 | Start Date*: 2021-11-22 |
Sponsor Name:NOEMI GUEMES VILLAHOZ | ||
Full Title: POST-MARKETING PARALLEL CLINICAL TRIAL TO DETERMINE THE EFFECTIVENESS AND TOLERABILITY OF DIMS LENSES IN THE CONTROL OF MYOPIA IN PEDIATRIC POPULATION | ||
Medical condition: MYOPIA IN PEDIATRIC POPULATION | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003376-14 | Sponsor Protocol Number: 1 | Start Date*: 2021-11-26 |
Sponsor Name:Mariano Artes Caselles | ||
Full Title: Efficacy of amoxicillin/clavulanic acid after surgical drainage of perianal abscess in the prevention of the development of anal fistula. A randomized, double-blind clinical trial. | ||
Medical condition: perianal abscess | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004506-21 | Sponsor Protocol Number: 21/2 | Start Date*: 2021-11-30 |
Sponsor Name:Hospital Universitario Fundación Alcorcón | ||
Full Title: ERECTOR SPINAE PLANE CATHETERS IN SCOLIOSIS SURGERY | ||
Medical condition: Postoperative pain following scoliosis surgery | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001579-35 | Sponsor Protocol Number: KBP5074-2-001 | Start Date*: 2019-08-07 | ||||||||||||||||
Sponsor Name:KBP BioSciences Co., Ltd. | ||||||||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Assess the Efficacy, Safety, and Pharmacokinetics of KBP-5074 in Patients with Moderate-to-Severe Chronic Kidney Disea... | ||||||||||||||||||
Medical condition: Moderate to Severe Chronic Kidney Disease and uncontrolled hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) BG (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003529-41 | Sponsor Protocol Number: ABR58805 | Start Date*: 2017-02-22 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: CANGLIA: Endocannabinoid control of microglia activation as a new therapeutic target in the treatment of schizophrenia | ||
Medical condition: Schizophrenia patients | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004282-31 | Sponsor Protocol Number: V14-11056 | Start Date*: 2017-03-15 | ||||||||||||||||
Sponsor Name:Vivolux AB | ||||||||||||||||||
Full Title: VLX1570 and Low-Dose Dexamethasone in Relapsed or Relapsed and Refractory Multiple Myeloma: A Clinical and Correlative Phase 1/2 Study | ||||||||||||||||||
Medical condition: Multiple Myeloma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001947-28 | Sponsor Protocol Number: T2017-002 | Start Date*: 2019-06-11 | ||||||||||||||||
Sponsor Name:Therapeutic Advances in Childhood Leukemia Consortium (TACL) | ||||||||||||||||||
Full Title: A TACL Phase 1/2 Study of PO Ixazomib in Combination with Chemotherapy for Childhood Relapsed or Refractory Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma | ||||||||||||||||||
Medical condition: Acute Lymphoblastic Leukemia (ALL) and Lymphoblastic Lymphoma (LLy) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003712-45 | Sponsor Protocol Number: INCB18424-303 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 3, Double-Blind, Randomized, 8-Week, Vehicle-Controlled Efficacy and Safety Study of Ruxolitinib Cream Followed by a Long Term Safety Extension Period in Adolescents and Adults With Atopic ... | |||||||||||||
Medical condition: Atopic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) FR (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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