- Trials with a EudraCT protocol (44,352)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,352 result(s) found.
Displaying page 356 of 2,218.
EudraCT Number: 2010-021022-35 | Sponsor Protocol Number: 0908125 | Start Date*: 2010-10-12 | ||||||||||||||||
Sponsor Name:CHU de Saint-Etienne | ||||||||||||||||||
Full Title: Effet of curarization under general anaesthesia on eye movements in non-strabismus children | ||||||||||||||||||
Medical condition: Healthy volunteer who will have a surgery requiring curare administration (amygdalectomy...) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021039-14 | Sponsor Protocol Number: S001-2010 | Start Date*: 2010-08-19 | ||||||||||||||||
Sponsor Name:Tampere University, Faculty of Medicine, Department of Ophthalmology | ||||||||||||||||||
Full Title: An open-label, phase IV, pilot study, to evaluate confocal microscopic findings of cornea, ocular signs and symptoms in patients with ocular hypertension or open-angle glaucoma switching from latan... | ||||||||||||||||||
Medical condition: Ocular Hypertension (OH) or Open-Angle Glaucoma (OAG); primary open-angle glaucoma [POAG] or capsular glaucoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021221-12 | Sponsor Protocol Number: UMC Utrecht | Start Date*: 2011-07-11 | |||||||||||
Sponsor Name:UMCU | |||||||||||||
Full Title: A phase I/ II study Efficacy and safety of alpha/beta T- /CD19B-cell depleted allogeneic haematopoietic stem cells transplantation in high risk or relapsed acute leukaemia / MDS followed by an inn... | |||||||||||||
Medical condition: Patients with high risk acute leukemia / MDS or relapse acute leukemia /MDS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001616-57 | Sponsor Protocol Number: ARD12130 | Start Date*: 2011-10-05 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Phase 2 study of SAR245409 in patients with relapsed or refractory mantle cell lymphoma, follicular lymphoma, or chronic lymphocytic leukemia/small lymphocytic lymphoma | |||||||||||||
Medical condition: Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021520-10 | Sponsor Protocol Number: D9830C00021 | Start Date*: 2010-09-16 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: An open, single centre, phase I study in male adolescents with asthma, aged 12 to 17 years, to assess pharmacokinetics of orally administered AZD1981 tablets 100mg twice daily for 6½ days | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021533-31 | Sponsor Protocol Number: CRIT124D2302 | Start Date*: 2011-02-08 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A 40-week, randomized, double-blind, placebo-controlled, multicenter efficacy and safety study of Ritalin® LA in the treatment of adult patients with childhood-onset ADHD | |||||||||||||||||||||||
Medical condition: Adult patients with childhood-onset Attention Deficit Hyperactivity Disorder | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) SE (Completed) BE (Completed) DK (Completed) NO (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021534-55 | Sponsor Protocol Number: 72311424 | Start Date*: 2010-12-16 | |||||||||||
Sponsor Name:Luis Carlos Imaz Navarro | |||||||||||||
Full Title: Comparación analgésica de bupivacaína, a diferentes dosis por catéter paravertebral torácico, y su implicación en la función pulmonar en pacientes intervenidos de toracotomía para cirugía de resecc... | |||||||||||||
Medical condition: Pacientes intervenidos de toracotomía para cirugía de resección pulmonar (Thoracotomy for pulmonar resection) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021456-25 | Sponsor Protocol Number: LAT-SOP-01-2010 | Start Date*: 2011-03-15 |
Sponsor Name:Laboratorios SOPHIA, S.A. de C.V. | ||
Full Title: ESTUDIO CLÍNICO DE SEGURIDAD PARA COMPARAR UNA SOLUCIÓN TÓPICA OFTÁLMICA DE GAAP OFTENO® (LATANOPROST AL 0.005%) FRENTE A XALATAN® (LATANOPROST AL 0.005%) COMO PRODUCTO DE REFERENCIA, EN PACIENTES... | ||
Medical condition: Pacientes con glaucoma primario de ángulo abierto y/o hipertensión ocular | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016953-16 | Sponsor Protocol Number: FTG-AD | Start Date*: 2010-07-14 |
Sponsor Name:Inn-Salzach-Klinikum gGmbH | ||
Full Title: Depressions-Spektrums-Störung und differenzielle Effekte neuerer Antidepressiva auf die Verkehrssicherheit | ||
Medical condition: Spectrum of depressive diseases, ICD-10: F32.x, F33.x | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016140-39 | Sponsor Protocol Number: IDI-GAD-2009-01 | Start Date*: 2010-01-19 |
Sponsor Name:Institut Diagnostic per la Imatge | ||
Full Title: MRI in Clinically Isolated Syndromes and relapsing multiple sclerosis after single dose (0.1 mmol/kg) and cumulative dose (0.1 + 0.1 mmol/kg) of GADOVIST at 3.0T Estudio de resonancia magnética 3... | ||
Medical condition: Realce de contraste en resonancia magnética en pacientes con Síndrome Clínico Aislado o recaída de Esclerosis Múltiple con resonancia magnética anormal anterior después de la administración de dosi... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021086-73 | Sponsor Protocol Number: Uni-Koeln-1443 | Start Date*: 2012-05-11 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: HD-R3i - A prospective, randomized, placebo-controlled, international, multicenter phase I/II trial of RAD001 (everolimus) in combination with DHAP as induction therapy in patients with relapsed or... | |||||||||||||
Medical condition: relapsed or refractory Hodgkin Lymphoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021092-89 | Sponsor Protocol Number: SICOG1001 | Start Date*: 2011-04-07 | |||||||||||
Sponsor Name:SOUTHERN ITALY COOPERATIVE ONCOLOGY GROUP | |||||||||||||
Full Title: Cisplatin and Alimta with panitumumaB for Advanced non-squamous Lung cAncer (CABALA Trial): a SICOG multicenter, phase II trial | |||||||||||||
Medical condition: previously untreated, EGFR + (FISH), advanced, non-squamous, NSCLC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021123-26 | Sponsor Protocol Number: 03062010 | Start Date*: 2010-10-29 | |||||||||||
Sponsor Name:National Institute for Health and Welfare | |||||||||||||
Full Title: Kaksoissokkoutettu kliininen hoitotutkimus: Rahapeliriippuvuuden hoitaminen opiaattisalpaaja naltreksonilla ja oppimismallilla | |||||||||||||
Medical condition: Pathological gambling dependence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001769-27 | Sponsor Protocol Number: CHI0465 | Start Date*: 2008-09-29 |
Sponsor Name:Southampton University Hospital Trust | ||
Full Title: Microbiological assessment of prophylactic ciprofloxacin therapy for children with cystic fibrosis during viral respiratory viral infection to prevent Pseudomonas aeruginosa colonisation – a random... | ||
Medical condition: Cystic Fibrosis Specifically the trial will include children aged 2-14 years with a diagnosis of cystic fibrosis and not chronically infected with pseudomonas aeruginosa in their lungs. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001774-32 | Sponsor Protocol Number: 880701 | Start Date*: 2008-06-04 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: A BLINDED PHASE I/II DOSE ESCALATION STUDY TO ASSESS SAFETY AND IMMUNOGENICITY AND INVESTIGATE THE OPTIMAL DOSE LEVEL OF A FORMALIN-TREATED, UV-INACTIVATED, VERO CELL-DERIVED ROSS RIVER VIRUS (RRV)... | |||||||||||||
Medical condition: Vaccination against Ross River Virus Infection in healthy subjects between 18-40 years of age. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001779-31 | Sponsor Protocol Number: FONDAPARINUX | Start Date*: 2008-05-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: Markers of hypercoagulability and risk of death and rehospitalization in heart failure patients: a pilot study on the effects of Fondaparinux | |||||||||||||
Medical condition: heart failure patients (III-IV NYHA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010434-22 | Sponsor Protocol Number: CCD-0902-PR-0013 | Start Date*: 2009-08-24 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A SINGLE-DOSE, OPEN-LABEL, 2-WAY CROSS-OVER, CLINICAL PHARMACOLOGY STUDY OF CHF 1535 50/6 HFA pMDI (FIXED COMBINATION OF BECLOMETHASONE DIPROPIONATE 50µg PLUS FORMOTEROL FUMARATE 6 µg ) USING THE A... | |||||||||||||
Medical condition: Asthmatic children, aged 5-11, with a forced expiratory volume in one second (FEV1) > 70% of predicted values. | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009952-18 | Sponsor Protocol Number: P071222 | Start Date*: 2010-01-05 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Intérêt des inhibiteurs de l'enzyme de conversion dans l'atteinte rénale précoce des enfants drépanocytaires : Etude randomisée en double aveugle énalapril versus placebo. | |||||||||||||
Medical condition: Atteinte rénale précoce des enfants drépanocytaires. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007177-20 | Sponsor Protocol Number: Sirolimus_Liver_Tolerance | Start Date*: 2009-09-07 | |||||||||||
Sponsor Name:Hospital Clinic Barcelona | |||||||||||||
Full Title: EFECTO DEL SIROLIMUS SOBRE LOS BIOMARCADORES RELACIONADOS CON LA TOLERANCIA EN RECEPTORES DE TRASPLANTE HEPÁTICO ESTABLES | |||||||||||||
Medical condition: Stable liver transplant recipients identified as non-tolerant (i.e. requiring indefinite immunosuppressive therapy) on the basis of peripheral blood transcriptional biomarkers. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007183-42 | Sponsor Protocol Number: A7881006 | Start Date*: 2009-03-20 | |||||||||||
Sponsor Name:Pfizer Ltd. | |||||||||||||
Full Title: A PHASE IIb RANDOMISED DOUBLE BLIND, PLACEBO CONTROLLED PARALLEL GROUP STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF PF-00610355 OVER 4 WEEKS IN MODERATE ASTHMATIC SUBJECTS | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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