- Trials with a EudraCT protocol (44,349)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,349 result(s) found.
Displaying page 993 of 2,218.
EudraCT Number: 2007-001013-41 | Sponsor Protocol Number: CIGE025A2210 | Start Date*: 2008-01-18 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, placebo-controlled study to demonstrate the efficacy of Xolair in an allergen bronchoprovocation study in two asthmatic populations defined by serum IgE concentrations | ||
Medical condition: Asthma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002074-58 | Sponsor Protocol Number: IIS-2007-01 | Start Date*: 2007-11-29 | |||||||||||
Sponsor Name:Instituto de Investigaciones del Sueño | |||||||||||||
Full Title: Estudio unicéntrico, aleatorizado, doble ciego, de diseño cruzado, controlado con placebo, de nueve semanas de duracion para evaluar la eficacia de oxibato sodico en pacientes con el síndrome de la... | |||||||||||||
Medical condition: El Síndrome de las piernas inquietas idiopático (SPI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000516-32 | Sponsor Protocol Number: LANTU_C_02761 | Start Date*: 2008-08-04 | |||||||||||
Sponsor Name:sanofi aventis Groupe | |||||||||||||
Full Title: Superiority study of insulin glargine over sitagliptin in insulin-naïve patients with type 2 diabetes treated with metformin and not adequately controlled | |||||||||||||
Medical condition: Type 2 diabetes treated with metformin and not adequately controlled | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) PT (Completed) AT (Completed) ES (Completed) GB (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007953-30 | Sponsor Protocol Number: cv-07/126 | Start Date*: 2008-02-11 |
Sponsor Name:Fundación Investigación y Desarrollo en el Área Cardiovascular | ||
Full Title: Levosimendan como agente inmunomodulador en la insuficiencia cardiaca aguda. Estudio Piloto Levosimendan as an immunomodulatory agent in acute heart failure. Pilot study. | ||
Medical condition: Analysis of the short-term treatment with levosimendan, a cardiac stimulant drug, of the acute exacerbation of chronic heart failure Estudio del tratamiento a corto plazo con levosimendan, fármac... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002223-32 | Sponsor Protocol Number: E2007-0507 | Start Date*: Information not available in EudraCT |
Sponsor Name:Charité Universitaetsmedizin | ||
Full Title: A multicentre, double-blind, randomised placebo-controlled trial of sodium bicarbonate to prevent acute kidney injury in patients undergoing cardiopulmonary bypass surgery. | ||
Medical condition: Cardiac surgical patients in whom the use of cardiopulmonary bypass is planned and having at least one ore more of the following risk factors for post-operative acute kidney injury • Age ≥ 70 years... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-004169-16 | Sponsor Protocol Number: ML20382 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Roche Farma, S.A. | |||||||||||||
Full Title: Estudio fase II multicéntrico, abierto, no aleatorizado para evaluar la eficacia de una combinación con bevacizumab y quimioterapia secuencial, como tratamiento de pacientes con cáncer de mama oper... | |||||||||||||
Medical condition: Adenocarcinoma de mama operable HER2 negativo, de más de 2 cm de tamaño, no tratado previamente. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004375-19 | Sponsor Protocol Number: TH0705 | Start Date*: 2007-10-26 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare | |||||||||||||
Full Title: A multi-centre, randomised, double-blind, parallel-group, placebo-controlled, multiple dose study of the efficacy of Strepsils original throat lozenges in the relief of sore throat due to upper res... | |||||||||||||
Medical condition: Sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007018-12 | Sponsor Protocol Number: QUINAVIR | Start Date*: 2008-06-23 | |||||||||||
Sponsor Name:Carlos Alonso-Villaverde Lozano, Hospital Universitari Sant Joan de Reus | |||||||||||||
Full Title: “Estudio prospectivo, abierto, aleatorizado y cruzado sobre el efecto de la Hidroxicloroquina, 200mg al día, en factores inflamatorios y metabólicos relacionados con la enfermedad cardiovascular en... | |||||||||||||
Medical condition: Infección por el virus de la inmunodeficiencia adquirida | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004370-55 | Sponsor Protocol Number: 2007-004370-55 | Start Date*: 2007-12-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA' GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Effects of tetrahydrobiopterin (6R-BH4) on flow-mediated dilation in CADASIL patients: a randomised controlled trial | |||||||||||||
Medical condition: CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy), is a rare autosomal dominant disorder characterized by recurrent strokes starting in mid-adulth... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006934-33 | Sponsor Protocol Number: 19.4.333 | Start Date*: 2008-04-02 |
Sponsor Name:NV Organon | ||
Full Title: A single center, open-label trial in subjects with severe renal impairment evaluating the dialysability of the sugammadex-rocuronium complex | ||
Medical condition: Not applicable | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003652-11 | Sponsor Protocol Number: NAI007 | Start Date*: 2008-09-01 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: A proof of concept study to evaluate the peak bronchoprotection conferred by single and chronic dosing with levosalbutamol and racemic salbutamol in persistent asthmatics. | |||||||||||||
Medical condition: Asthma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005958-23 | Sponsor Protocol Number: Y-47-52120-128 | Start Date*: 2008-03-03 | |||||||||||
Sponsor Name:Ipsen Group, SCRAS Institut Henri Beaufour | |||||||||||||
Full Title: A Phase II, Randomised, Double-Blind Study to Compare the Safety and Efficacy of One Treatment Cycle of Clostridium Botulinum Type A Toxin (50 Units) When Reconstituted from Either a 125 Unit or a ... | |||||||||||||
Medical condition: Moderate to severe vertical glabellar lines. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001676-36 | Sponsor Protocol Number: 3066001 | Start Date*: 2007-12-18 | |||||||||||
Sponsor Name:ORION PHARMA | |||||||||||||
Full Title: Non-inferiority study; Comparison of polyethylene glycol solution with and without electrolytes for treatment of chronic constipation in elderly institutionalised patients: a double-blind, randomis... | |||||||||||||
Medical condition: Constipation | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005737-11 | Sponsor Protocol Number: PH-L19IL2 DTIC - 03/07 | Start Date*: 2008-01-17 | |||||||||||
Sponsor Name:PHILOGEN S.P.A. | |||||||||||||
Full Title: Dose definition and activity evaluation study of the tumor-targeting human L19IL2 monoclonal antibody-cytokine fusion protein in combination with Dacarbazine in patients with metastatic melanoma | |||||||||||||
Medical condition: unresectable metastatic (stage IV)non-uveal melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006190-87 | Sponsor Protocol Number: CTOM01 | Start Date*: 2008-03-04 | |||||||||||
Sponsor Name:Omega Pharma N.V. | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, clinical trial to investigate superiority of Lyclear spray away (ParaNix spray) compared with Infectopedicul permethrin 0.5% lotion in the treatment of hea... | |||||||||||||
Medical condition: Infestation by head lice (pediculosis capitis) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004761-17 | Sponsor Protocol Number: SG033-0003 | Start Date*: 2008-05-14 | |||||||||||
Sponsor Name:Seattle Genetics, Inc. | |||||||||||||
Full Title: A Phase IIB, Randomized, Double-Blinded, Placebo-Controlled Study of Low Dose Cytarabine and Lintuzumab Compared to Low Dose Cytarabine and Placebo in Patients 60 Years of Age and Older with Previo... | |||||||||||||
Medical condition: acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) HU (Prematurely Ended) AT (Completed) PL (Prematurely Ended) BG (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004779-21 | Sponsor Protocol Number: BA058-05-002 | Start Date*: 2007-12-07 | |||||||||||
Sponsor Name:Radius Health, Inc | |||||||||||||
Full Title: A Randomized, Parallel-Group, Phase 2 Dose-finding Study to Evaluate the Effects of BA058 in the Treatment of Postmenopausal Women with Osteoporosis | |||||||||||||
Medical condition: Osteoporosis in postmenopausal women. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-003432-22 | Sponsor Protocol Number: EGF104383 | Start Date*: 2008-07-03 | |||||||||||
Sponsor Name:Glaxo SmithKline Research and Development Limited | |||||||||||||
Full Title: A Randomized, Double Blind, Placebo-Controlled, Multicenter, Phase III Study Comparing the Activity of Paclitaxel Plus Trastuzumab Plus Lapatinib to Paclitaxel Plus Trastuzumab Plus Placebo in Wome... | |||||||||||||
Medical condition: ErbB2+ Metastatic Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007673-23 | Sponsor Protocol Number: 07/H0308/171 | Start Date*: 2008-03-12 | |||||||||||
Sponsor Name:Cambridge University Hospitals Foundation Trust | |||||||||||||
Full Title: Evaluation of carotid atheroma with contrast enhanced magnetic resonance imaging | |||||||||||||
Medical condition: Carotid artery atheroma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003250-29 | Sponsor Protocol Number: IPAB-07-002 | Start Date*: 2008-03-14 | |||||||||||
Sponsor Name:Independent Pharmaceutica AB | |||||||||||||
Full Title: A randomised, placebo-controlled, multi-centre study on the efficacy of Niccine, a vaccine for nicotine, in smoking relapse prevention, assessed in abstinent, adult smokers. | |||||||||||||
Medical condition: The intended indication for the drug under investigation is smoking relapse prevention. Tobacco smoking has been identified as the single largest preventable cause of morbidity and premature death ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
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