- Trials with a EudraCT protocol (44,336)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,336 result(s) found.
Displaying page 214 of 2,217.
EudraCT Number: 2007-002463-27 | Sponsor Protocol Number: LY/AP-01/2007 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Lybar a.s. | |||||||||||||
Full Title: Clinical study phase III evaluating the safety of Diffusil H Forte spray. | |||||||||||||
Medical condition: This is an open-label clinical study evaluating the safety of Diffusil H Forte spray in people with pediculosis or in increased risk of infection of pediculosis. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012596-94 | Sponsor Protocol Number: GRACIA-4 | Start Date*: 2009-11-10 |
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Gregorio Marañón | ||
Full Title: Estudio clínico aleatorizado comparativo entre angioplastia primaria y angioplastia postfibrinolisis como estrategias de reperfusión en pacientes con infarto agudo de miocardio con elevación del se... | ||
Medical condition: La hipótesis conceptual de este estudio es que en los pacientes con infarto agudo de miocardio y segmento ST elevado la angioplastia primaria es superior a una estrategia mixta de fibrinolisis inme... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006187-35 | Sponsor Protocol Number: 0974-016 | Start Date*: 2007-04-10 | |||||||||||
Sponsor Name:Laboratoires Merck Sharp & Dohme - Chibret | |||||||||||||
Full Title: A phase III, Multicenter, Randomized, Placebo-Controlled Clinical Trial to Study the Safety and Efficacy of Oral MK-0974 in the Acute Treatment of Migraine with or Without Aura. | |||||||||||||
Medical condition: Acute treatment of Migraine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006189-40 | Sponsor Protocol Number: GIMEMA CML0206 | Start Date*: 2007-03-27 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL ADULTO | |||||||||||||
Full Title: PHASE II MULTICENTER STUDY OF P210-B3A2 DERIVED PEPTIDE VACCINE IN CHRONIC MYELOID LEUKEMIA PATIENTS IN COMPLETE CYTOGENETIC RESPONSE WITH PERSISTENT MOLECULAR RESIDUAL DISEASE DURING IMATINIB TREA... | |||||||||||||
Medical condition: CHRONIC MYELOID LEUKEMIA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006191-38 | Sponsor Protocol Number: 004SC06084 | Start Date*: 2007-01-11 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: The effects of the association bindarit irbesartan versus irbesartan alone on albuminuria of patients with Diabetic Nephropathy. Placebo-controlled study. | |||||||||||||
Medical condition: Patients with type II diabetes with nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006198-26 | Sponsor Protocol Number: SAG-44/DIV | Start Date*: 2007-07-23 |
Sponsor Name:University of Nottingham | ||
Full Title: Mechanistic randomised contorlled trial of Mesalazine in symptomatic diverticular disease | ||
Medical condition: Symptomatic diverticular disease defines as patients with recurrent abdominal pain on more then 3 days per month with proven diverticula. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-007829-40 | Sponsor Protocol Number: DAM/003/08 | Start Date*: 2009-01-29 | |||||||||||
Sponsor Name:FARMACEUTICI DAMOR | |||||||||||||
Full Title: Open-label, controlled, randomised, single centre, parallel group clinical trial of efficacy and tolerability of Clarema 1% cream and Hirudoid 40000 U.APTT gel in the topical treatment of haematoma... | |||||||||||||
Medical condition: Patients with haematomas and subcutaneous haematic extravasations of traumatic origin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011041-12 | Sponsor Protocol Number: ET-A-018-09 | Start Date*: 2009-07-23 | |||||||||||
Sponsor Name:Pharma Mar S.A. | |||||||||||||
Full Title: Étude multicentrique de phase Ib-II en escalade de dose de la trabectédine (Yondelis®) en association avec l’oxaliplatine chez des patientes atteintes d’un cancer de l’ovaire avancé prétraité. | |||||||||||||
Medical condition: Pretreated Advanced Ovarian Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007645-31 | Sponsor Protocol Number: 00591 | Start Date*: 2009-06-23 | |||||||||||
Sponsor Name:University Medical Center Freiburg | |||||||||||||
Full Title: Freiburger Studie zur Behandlung von Primären ZNS-Lymphomen bei Patienten über 65 Jahre: Methotrexat-basierte Chemo-Immuntherapie mit anschließender Erhaltungstherapie - PRIMAIN-Studie - | |||||||||||||
Medical condition: Patients with primary CNS Lymphoma | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015743-16 | Sponsor Protocol Number: NA | Start Date*: 2009-10-09 |
Sponsor Name:University Hospitals of Leicester NHS Trust | ||
Full Title: A randomised, partially observer-blind, multi-centre, head-to-head comparison of a two dose regimen of Baxter and GSK H1N1 pandemic vaccines, administered 21 days apart | ||
Medical condition: Pandemic H1N1 influenza. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015749-22 | Sponsor Protocol Number: ADATOP | Start Date*: 2010-12-22 | |||||||||||
Sponsor Name:University of Leipzig | |||||||||||||
Full Title: A prospective, monocentric clinical trial with adalimumab for topical treatment in chronic wounds | |||||||||||||
Medical condition: Chronic stasis ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015760-33 | Sponsor Protocol Number: P090303 | Start Date*: 2009-11-17 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Effet de différents schémas d'insulinothérapie sur la compliance artérielle, la fonction endothéliale et la fonction autonome cardiaque de patients diabétiques de type 2 mal équilibrés sous traitem... | |||||||||||||
Medical condition: Diabéte de type 2 mal équilibré | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015770-35 | Sponsor Protocol Number: 1230.18 | Start Date*: 2010-03-17 |
Sponsor Name:Boehringer Ingelheim France | ||
Full Title: Phase II randomized trial of the Polo-like kinase 1 inhibitor BI 6727 monotherapy versus investigator’s choice chemotherapy in ovarian cancer patients resistant or refractory to platinum-based cyto... | ||
Medical condition: Recurrent ovarian cancer resistant or refractory to platinum compounds | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FR (Completed) ES (Completed) BE (Completed) SE (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001053-18 | Sponsor Protocol Number: IC 2007-04 | Start Date*: 2008-05-29 |
Sponsor Name:INSTITUT CURIE | ||
Full Title: Étude de phase II randomisée évaluant une irradiation pelvienne associée au Cisplatine seul ou au Cisplatine plus Cetuximab chez des patientes présentant un carcinome du col utérin de stade IB2, II... | ||
Medical condition: Patientes présentant un cancer du col de l’utérus de type épidermoïde ou adénocarcinome de stade Ib2 à IIIb, non antérieurement traitées. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016661-28 | Sponsor Protocol Number: TTD-09-03 | Start Date*: 2010-03-16 |
Sponsor Name:Grupo Español de Tratamiento de Tumores Digestivos-TTD | ||
Full Title: Estudio de fase II de panitumumab como agente único de primera línea en pacientes ancianos frágiles con cáncer colorrectal avanzado con KRAS no mutado | ||
Medical condition: Estudio de fase II de panitumumab como agente único de primera línea en pacientes ancianos frágiles con cáncer colorrectal avanzado con KRAS no mutado | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016684-11 | Sponsor Protocol Number: meloxicam09 | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | |||||||||||||
Full Title: Meloxicam periradicular injection in physiological solution vs physiological solution in the treatment of lumbar and/or sacral radiculite: single blind randomized study | |||||||||||||
Medical condition: patients with radiculite lumbar and/or sacral pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016690-15 | Sponsor Protocol Number: AC4113589 | Start Date*: 2010-02-12 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development LTD | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, placebo-controlled study to evaluate the efficacy and safety of GSK573719 delivered once-daily over 28 days in subjects with COPD | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011424-64 | Sponsor Protocol Number: M10-984 | Start Date*: 2009-11-09 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo- and Active-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of ABT-126 in Subjects with Mild-to-Moderate Alzheimer's Disease | |||||||||||||
Medical condition: Mild to moderate Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) GB (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005912-41 | Sponsor Protocol Number: TMO-07001 | Start Date*: 2010-05-04 | ||||||||||||||||
Sponsor Name:Belpharma SA/NV | ||||||||||||||||||
Full Title: Temocillin use in Complicated Urinary Tract Infections due to ESBL producing and AmpC hyperproducing Enterobacteriaceae in United Kingdom | ||||||||||||||||||
Medical condition: Patients presenting urinary tract infections due to Extended Spectrum Beta-Lactamases producing or AmpC hyperproducing Enterobacteriaceae. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005929-11 | Sponsor Protocol Number: CN156013 | Start Date*: 2009-02-20 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Multicenter, Randomized Double-Blind Placebo-Controlled Study of the Safety, Tolerability, Pharmacodynamic and Pharmacokinetic Effects of BMS-708163 in the Treatment of Patients with Mild to Mode... | |||||||||||||
Medical condition: ALZHEIMER DISEASE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
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