- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 462 of 2,219.
| EudraCT Number: 2013-002214-13 | Sponsor Protocol Number: IIBSP-OXI-2013-62 | Start Date*: 2013-10-28 |
| Sponsor Name:Institut de Recerca de l?Hospital de la Santa Creu i Sant Pau ? IIB Sant Pau | ||
| Full Title: Evaluation of oxidative stress associated with the administration of two different concentrations of oxygen for the maintenance of general anesthesia | ||
| Medical condition: General anesthesia and oxidative stress | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-002258-60 | Sponsor Protocol Number: UMCN-ONCO-201302 | Start Date*: 2013-08-30 | |||||||||||
| Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
| Full Title: prediction of everolimus-induced interstitial lung disease in breast cancer patients; maximizing efficacy by reducing toxicity | |||||||||||||
| Medical condition: breast cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005529-34 | Sponsor Protocol Number: TRx-237-007 | Start Date*: 2012-12-28 | |||||||||||
| Sponsor Name:TauRx Therapeutics Ltd | |||||||||||||
| Full Title: A Double-Blind, Placebo-Controlled, Randomized, Parallel Group, 12-Month Safety and Efficacy Trial of Leuco-methylthioninium bis(hydromethanesulfonate) in Subjects with Behavioral Variant Frontotem... | |||||||||||||
| Medical condition: behavioral variant Frontotemporal Dementia (bvFTD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) NL (Completed) IT (Completed) FI (Completed) PL (Completed) ES (Completed) HR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005537-39 | Sponsor Protocol Number: LEGA | Start Date*: 2012-04-18 | |||||||||||
| Sponsor Name:GISCAD | |||||||||||||
| Full Title: A Randomized Phase III Study Of Low-Docetaxel Oxaliplatin, Capecitabine (Low-Tox) Vs Epirubicin, Oxaliplatin And Capecitabine (Eox) In Patients With Locally Advanced Unresectable Or Metastatic Gast... | |||||||||||||
| Medical condition: Locally advanced unresectable or metastatic gastric cancer. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005544-10 | Sponsor Protocol Number: NIHRCDF | Start Date*: 2012-04-10 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: Improving Inhaler Treatment and Small Airways Assessment in Chronic Obstructive Pulmonary Disease | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005575-16 | Sponsor Protocol Number: BufferedTumescenceV3 | Start Date*: 2011-12-21 |
| Sponsor Name:Hull & East Yorkshire Hospitals NHS Trust | ||
| Full Title: Tumescent Anaesthesia in Endovenous Laser Ablation of Varicose Veins: A Randomised Controlled Trial of a Buffered Tumescent Solution | ||
| Medical condition: Pain of injection of a tumescent anaesthetic solution used during EndoVenous Laser Ablation of Varicose Veins. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005586-21 | Sponsor Protocol Number: GMX02 | Start Date*: 2011-12-07 | |||||||||||
| Sponsor Name:Bio Products Laboratory Limited | |||||||||||||
| Full Title: A Phase III, Multicenter, Open-Label Study To Evaluate the Efficacy and Safety of GAMMAPLEX® in Chronic Idiopathic Thrombocytopenic Purpura | |||||||||||||
| Medical condition: Idiopathic thrombocytopenic purpura. | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003110-14 | Sponsor Protocol Number: MK-0859-021 | Start Date*: 2012-12-03 |
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | ||
| Full Title: A 24-Week, Worldwide, Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Assess the Efficacy and Tolerability of Anacetrapib When Added to Ongoing Statin Therapy With or W... | ||
| Medical condition: Hypercholesterolemia or Low HDL-C | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) GB (Completed) DE (Completed) HU (Completed) ES (Completed) SK (Completed) BG (Completed) RO (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000174-37 | Sponsor Protocol Number: GEICAM/2011-03_S1007 | Start Date*: 2012-04-26 | |||||||||||
| Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | |||||||||||||
| Full Title: A Phase III, Randomized Clinical Trial of Standard Adjuvant Endocrine Therapy +/- Chemotherapy in Patients with 1-3 Positive Nodes, Hormone Receptor-Positive and HER2-Negative Breast Cancer with Re... | |||||||||||||
| Medical condition: Patients with confirmed diagnosis of node positive (1-3 nodes) invasive breast carcinoma with positive hormone receptor status, and negative HER-2. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000181-37 | Sponsor Protocol Number: CVT-301-002 | Start Date*: 2012-04-25 | |||||||||||
| Sponsor Name:Civitas Therapeutics, Inc. | |||||||||||||
| Full Title: A Randomized, Placebo-Controlled Phase 2 Study of the Safety, Pharmacokinetics, and Pharmacodynamics of CVT-301 (Levodopa Inhalation Powder) in Patients with Parkinson’s Disease and Motor Response ... | |||||||||||||
| Medical condition: Parkinson's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000215-89 | Sponsor Protocol Number: CL2-16257-099 | Start Date*: 2013-06-14 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: Effects of ivabradine on vascular function in individuals at increased risk of developing cardiovascular disease and with impaired endothelial function An international, multicentre, randomised, d... | |||||||||||||
| Medical condition: Cardiovascular disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019962-10 | Sponsor Protocol Number: P1-SAF301 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:SANFILIPPO Therapeutics SAS | |||||||||||||
| Full Title: AN OPEN-LABEL, SINGLE ARM, MONOCENTRIC, PHASE I/II CLINICAL STUDY OF INTRACEREBRAL ADMINISTRATION OF ADENO-ASSOCIATED VIRAL VECTORS SEROTYPE 10 CARRYING THE HUMAN SGSH AND SUMF1 cDNAS FOR THE TREAT... | |||||||||||||
| Medical condition: Sanfilippo type A syndrome (also named Mucopolysaccharidosis Type A) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004851-35 | Sponsor Protocol Number: T1040G0013 | Start Date*: 2012-12-19 | |||||||||||
| Sponsor Name:Children´s Hospital, University of Helsinki | |||||||||||||
| Full Title: Once versus twice daily mesalazine to introduce remission in pediatric ulcerative colitis: a randomized controlled trial | |||||||||||||
| Medical condition: Ulcerative colitis | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004884-29 | Sponsor Protocol Number: 12-BI-505-02 | Start Date*: 2013-01-16 | |||||||||||
| Sponsor Name:BioInvent International AB | |||||||||||||
| Full Title: A single-arm, Open-label, Phase 2 Clinical Trial Evaluating Disease Response Following Treatment With BI-505, a Human Anti–Intercellular Adhesion Molecule 1 Monoclonal Antibody, In Patients With Sm... | |||||||||||||
| Medical condition: Smoldering (asymptomatic) multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-003482-18 | Sponsor Protocol Number: RN01-CP-0002 | Start Date*: 2014-03-24 | |||||||||||
| Sponsor Name:ReNeuron Ltd | |||||||||||||
| Full Title: A Phase II Efficacy Study of Intracerebral CTX0E03 DP In Patients with Stable Paresis of the Arm Following an Ischaemic Stroke. | |||||||||||||
| Medical condition: Supratentorial ischaemic stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001307-20 | Sponsor Protocol Number: CNIO-GI-01-2012 | Start Date*: 2012-07-04 | |||||||||||
| Sponsor Name:Fundación Centro Nacional de Investigaciones Oncológicas Carlos III (CNIO) | |||||||||||||
| Full Title: Selection of Individualize Therapy in Metastatic Colon Cancer Patients According to the Genome Expression Profile in Tumor Samples. | |||||||||||||
| Medical condition: Metastatic Colon Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001324-34 | Sponsor Protocol Number: C-12-008 | Start Date*: 2013-03-07 |
| Sponsor Name:Alcon Research Ltd | ||
| Full Title: A 3 Month, Multicenter, Double-Masked Safety and Efficacy Study of Travoprost Ophthalmic Solution, 0.004% Compared to Timolol (0.5% or 0.25%) in Pediatric Glaucoma Patients | ||
| Medical condition: Pediatric glaucoma;elevated intraocular pressure | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: BE (Completed) GB (Completed) PL (Completed) DE (Completed) PT (Completed) NL (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-001327-12 | Sponsor Protocol Number: FIBHGM-ECNC001-2012 | Start Date*: 2012-11-19 | |||||||||||
| Sponsor Name:Fundacion para la Investigación Biomédica del Hospital Gregorio Marañón | |||||||||||||
| Full Title: Assessing the efficacy and toxicity of intravenous immunoglobulin for the treatment of infections in patients with post solid organ transplantation IgG hypogammaglobulinemia | |||||||||||||
| Medical condition: infections in patients with post solid organ transplantation IgG hypogammaglobulinemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001344-22 | Sponsor Protocol Number: 116640 | Start Date*: 2013-02-19 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A phase II, randomised, single-blind study to develop read-outs aimed at detecting and characterising the early and adaptive immune responses and to evaluate the kinetics of the early response and ... | ||
| Medical condition: Healthy volunteers (Hepatitis B surface antigen (HBsAg) vaccine administered in hepatitis B virus (HBV) naive adult subjects aged between 18 and 45 years old, inclusive, in good general health.) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000586-37 | Sponsor Protocol Number: BACSARM | Start Date*: 2013-09-23 |
| Sponsor Name:Miquel Pujol Rojo (Infectious Diseases Service-Hospital Universitari de Bellvitge-IDIBELL) | ||
| Full Title: Randomized multicenter study to assess efficacy of Daptomycin plus Fosfomycin versus Daptomycin monotherapy for treatment of methicillin resistant Staphylococcus aureus bacteremia in hospitalized p... | ||
| Medical condition: Methicillin resistant Staphylococcus aureus bacteremia, complicated or uncomplicated | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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