- Trials with a EudraCT protocol (26,035)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
26,035 result(s) found.
Displaying page 720 of 1,302.
EudraCT Number: 2012-004583-22 | Sponsor Protocol Number: 548.12 | Start Date*: 2012-10-20 | |||||||||||
Sponsor Name:OSPEDALE PEDIATRICO BAMBINO GESU' DI ROMA | |||||||||||||
Full Title: Verification of the effectiveness of intravenous sildenafil compared to other pulmonary vasodilators used in the test vessel reactivity of pulmonary | |||||||||||||
Medical condition: Subjects in children with congenital heart disease surgery or not, with echocardiographic signs of pulmonary hypertension followed at the Pediatric Cardiology Centre of the Mediterranean or reporte... | |||||||||||||
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Population Age: In utero, Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006329-42 | Sponsor Protocol Number: CAD0111 | Start Date*: 2012-10-11 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: Short course of Bortezomib in anemic patients with refractory cold agglutinin disease | |||||||||||||
Medical condition: Anaemia with refractory cold agglutinin disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020404-29 | Sponsor Protocol Number: H9V-MC-GFRF | Start Date*: 2011-04-08 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited, Indianapolis | |||||||||||||
Full Title: A Randomized, Double-Masked, Placebo-Controlled, Multicenter, Phase 2 Study to Evaluate the Safety and Renal Efficacy of LY2382770 in Patients with Diabetic Kidney Disease due to Type 1 or Type 2 D... | |||||||||||||
Medical condition: Patients with Diabetic Kidney Disease due to Type 1 or Type 2 Diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023792-25 | Sponsor Protocol Number: HTA08/14/39 | Start Date*: 2011-02-10 | |||||||||||
Sponsor Name:Alder Hey Children's NHS Foundation Trust | |||||||||||||
Full Title: A randomised controlled trial of continuous subcutaneous insulin infusion(CSII) compared to multiple daily injection(MDI) regimens on insulin in children and young people at diagnosis of type I dia... | |||||||||||||
Medical condition: Type 1 Diabetes Mellitus | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003266-32 | Sponsor Protocol Number: A0081269 | Start Date*: 2011-12-21 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 3B MULTICENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED CROSS-OVER EFFICACY AND SAFETY STUDY OF PREGABALIN IN THE TREATMENT OF PATIENTS WITH PAINFUL DIABETIC PERIPHERAL NEUROPATHY AND ... | |||||||||||||
Medical condition: Painful Diabetic Peripheral Neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004130-34 | Sponsor Protocol Number: EFC11569 | Start Date*: 2012-10-17 | |||||||||||
Sponsor Name:sanofi-aventis Recherche & Développement | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group Study to Evaluate the Efficacy and Safety of SAR236553/REGN727 Versus Ezetimibe in High Cardiovascular Risk Patients With Hypercholesterolemia Not Adequat... | |||||||||||||
Medical condition: Hypercholesterolaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DK (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002608-42 | Sponsor Protocol Number: PD0004 | Start Date*: 2013-01-10 | |||||||||||
Sponsor Name:UCB Biosciences GmbH | |||||||||||||
Full Title: A Multicenter, Multinational, Double-blind, Placebo-controlled, 2-arm Study to Evaluate the Efficacy of Rotigotine on Parkinson's Disease-Associated Pain | |||||||||||||
Medical condition: Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002007-15 | Sponsor Protocol Number: AXL-003 | Start Date*: 2011-10-12 | ||||||||||||||||
Sponsor Name:Axelar AB | ||||||||||||||||||
Full Title: Phase II, randomized, open-label study of the IGF-1R inhibitor AXL1717 compared to docetaxel in patients with previously treated, locally advanced, or metastatic squamous cell carcinoma or adenocar... | ||||||||||||||||||
Medical condition: Non-small-cell lung cancer previously treated | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001732-37 | Sponsor Protocol Number: TAK-875_306 | Start Date*: 2012-08-29 | |||||||||||||||||||||||||||||||
Sponsor Name:Takeda Global Research & Development Centre (Europe) Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate Cardiovascular Outcomes of TAK-875, 50 mg in Addition to Standard of Care in Subjects with Type 2 Diabetes and... | |||||||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes mellitus (T2DM) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) DE (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) LV (Prematurely Ended) GB (Completed) IT (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000789-39 | Sponsor Protocol Number: 116663 | Start Date*: 2012-06-28 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A Phase III, open, non-randomized, multi-centre, single dose study to assess immunogenicity and safety of Fluarix/Influsplit SSW 2012/2013 injected intramuscularly in adults (18 to 60 years) and in... | |||||||||||||
Medical condition: Immunization against Influenza of healthy adults | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002495-13 | Sponsor Protocol Number: SPD555-403 | Start Date*: 2013-01-14 |
Sponsor Name:Shire-Movetis NV | ||
Full Title: An Open-label, Randomized, Crossover, Reader-blinded Study To Investigate the Effect of Prucalopride and Polyethylene Glycol 3350 on Colon Motility with Intraluminal Manometry in Subjects with C... | ||
Medical condition: Chronic Constipation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001813-17 | Sponsor Protocol Number: R1282 | Start Date*: 2012-08-06 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | ||||||||||||||||||||||||||||||||||||||
Full Title: Study of apoptosis related changes and endothelial responses of multiple myeloma patients treated with chemotherapy. | ||||||||||||||||||||||||||||||||||||||
Medical condition: Chemotherapy related thrombosis in patients treated for multiple myeloma. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000622-22 | Sponsor Protocol Number: ASAP | Start Date*: 2012-07-20 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Aspirin for the enhancement of trophoblastic invasion in women with abnormal uterine artery Doppler at 11-14 weeks of gestation | |||||||||||||
Medical condition: Placental insufficiency | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003595-36 | Sponsor Protocol Number: ERN_11-0670 | Start Date*: 2012-04-26 |
Sponsor Name:University of Birmingham | ||
Full Title: Can muscle dysfunction in COPD be altered by oxygenation in patients with intermittent hypoxia on exertion? | ||
Medical condition: Chronic obstructive pulmonary disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001709-26 | Sponsor Protocol Number: IMS012012 | Start Date*: 2012-06-28 | |||||||||||
Sponsor Name:Sevapharma,a.s. | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled clinical trial of Immodin immunological efficacy in healthy adult volunteers. | |||||||||||||
Medical condition: Immunological efficacy, in healthy volunteers | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002430-36 | Sponsor Protocol Number: AntibioTICS | Start Date*: 2012-07-02 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Multicentre, randomised, double-blinded, placebo-controlled trial of efficacy of amoxicilline/clavulanic acid in patients affected by tic disorder colonized by GAS. No-proft stidy. | |||||||||||||
Medical condition: Chronic tic disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) ES (Ongoing) NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002545-35 | Sponsor Protocol Number: OCTO_026 | Start Date*: 2012-01-23 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: A randomised phase 2 study of paclitaxel with or without GSK1120212 in advanced wt BRAF melanoma | |||||||||||||
Medical condition: Advanced/metastatic melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006275-20 | Sponsor Protocol Number: LP0074-33 | Start Date*: 2012-08-20 | ||||||||||||||||
Sponsor Name:LEO Pharma A/S | ||||||||||||||||||
Full Title: A phase II exploratory study evaluating the efficacy of topical cromoglicate solution(20mg/ml) compared to topical solution vehicle in the treatment of mastocytosis | ||||||||||||||||||
Medical condition: mastocytosis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003826-28 | Sponsor Protocol Number: Z7190L01 | Start Date*: 2012-10-03 | ||||||||||||||||
Sponsor Name:ZAMBON S.p.A. | ||||||||||||||||||
Full Title: Evaluation of efficacy and safety of Ibuprofen Arginine 600 mg tid vs. Ibuprofen 600 mg tid in the treatment of pain and inflammation in Osteoarthritis (OA) patients with hypertension pharmacologic... | ||||||||||||||||||
Medical condition: Osteoarthritis of the knee or hip that requires taking NSAIDs for at least 14 days and hypertension stabilized with drugs. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004185-14 | Sponsor Protocol Number: CDPG103ADE01 | Start Date*: 2012-02-29 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy and safety of intraseasonal specific short-term immunotherapy with depigmented glutaraldeh... | |||||||||||||||||||||||
Medical condition: Allergic rhinitis and/or rhinoconjunctivitis with or without intermittent asthma. | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
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