- Trials with a EudraCT protocol (44,396)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,396 result(s) found.
Displaying page 152 of 2,220.
| EudraCT Number: 2006-003322-28 | Sponsor Protocol Number: BUP4006 | Start Date*: 2007-06-21 |
| Sponsor Name:Norpharma A/S | ||
| Full Title: A randomised, double-blind, multicentre non-inferiority study with active, parallel comparator group, to evaluate the efficacy and safety of Norspan® versus Tramadol in subjects with chronic, mode... | ||
| Medical condition: Chronic, moderate to severe osteoarthritis in hip, knee and/or lumbar spine | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001321-25 | Sponsor Protocol Number: Adenosin, låg- och högdos | Start Date*: 2006-05-22 |
| Sponsor Name:Karolinska Universitetssjukhuset | ||
| Full Title: Prövning av hypotesen att lågdosinfusion av adenosin hos patienter med ischemisk hjärtsjukdom har en prekonditionerande effekt. En placebokontrollerad crossover-studie. | ||
| Medical condition: Patienter med konstaterad kranskärlssjukdom, dvs signifikanta stenoser enl koronarangiografi (LAD-stenos eller 3-kärlssjukdom). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001786-34 | Sponsor Protocol Number: IT-04-01 | Start Date*: 2005-05-16 | |||||||||||
| Sponsor Name:ALCON ITALIA | |||||||||||||
| Full Title: Hypotonic efficacy and tollerability of Travoprost in patient with open angle primary glaucoma and/or ocular hypertension, not controlled with dorzolamide + timolol treatment in fixed association... | |||||||||||||
| Medical condition: Reducing high intraocular pressure in patient with ocular hypertension or open-angle glaucoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000983-29 | Sponsor Protocol Number: MA 17502 | Start Date*: 2005-01-12 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
| Full Title: Effectiveness of a once weekly subcutaneous epoetin beta treatment in hemodialysis patients. | |||||||||||||
| Medical condition: Renal anemia in hemodialysis patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004752-13 | Sponsor Protocol Number: MAR-LEV-2005-01 | Start Date*: 2006-05-25 |
| Sponsor Name:H. Universitari Germans Trias i Pujol | ||
| Full Title: Comparación cruzada, a doble ciego, aleatoria, de dosis única, de levocetirizina con desloratadina, rupatadina, ebastina y placebo: supresión de la respuesta de pápula y eritema inducida por histam... | ||
| Medical condition: Rinitis alérgica estacional | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002074-22 | Sponsor Protocol Number: UM2005/00201/00 | Start Date*: 2006-10-18 |
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | ||
| Full Title: A Randomized, Phase III, Open-Label Study of Oral Topotecan Plus Whole-Brain Radiation Therapy (WBRT) Compared with WBRT Alone in Patients with Brain Metastases from Non-Small Cell Lung Cancer. | ||
| Medical condition: Brain metastases from primary non-small cell lung cancer (NSCLC). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) SK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000727-42 | Sponsor Protocol Number: CYT004-MelQbG10 01 | Start Date*: 2006-01-20 |
| Sponsor Name:Cytos Biotechnology AG | ||
| Full Title: A Phase IIa Study to Evaluate Safety, Tolerability, and Immunogenicity of a Melan-A-VLP Vaccine in HLA-A2 Positive Patients with stage III/IV Malignant Melanoma | ||
| Medical condition: Patients with Stage III/IV Malignant Melanoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000730-20 | Sponsor Protocol Number: FP-001-IM | Start Date*: 2006-02-02 | |||||||||||
| Sponsor Name:Nycomed Danmark Aps | |||||||||||||
| Full Title: An open label, international, multi centre, parallel group, phase III b, randomised trial, investigating lumbar spine Bone Mineral Density (BMD) changes in postmenopausal women with primary osteopo... | |||||||||||||
| Medical condition: Primary postmenopausal osteoporosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000737-38 | Sponsor Protocol Number: TS2005 | Start Date*: 2005-05-31 |
| Sponsor Name:RAFAEL GARCIA LOPEZ | ||
| Full Title: NUEVOS ENFOQUES TERAPEUTICOS PARA EL SINDROME DE TOURETTE EN NIÑOS: Estudio fase II para conocer la eficacia y la seguridad del Magnesio y Vitamina B6 para el tratamiento del Síndrome de Tourette ... | ||
| Medical condition: Síndrome de Tourette Tics motores múltiples y uno o más tics vocales, presentes en algún momento durante la enfermedad, aunque no necesariamente al mismo tiempo. Los tics ocurren muchas veces a... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003115-74 | Sponsor Protocol Number: SM4-05 | Start Date*: 2005-10-24 |
| Sponsor Name:Dept. of Anaestesiology, University hospital in Glostrup | ||
| Full Title: Effect of paracetamol versus paracetamol combined with pregabalin versus paracetamol combined with pregabalin and dexamethason on pain and opiod requirements in patient sheduled for tonsilectomie | ||
| Medical condition: Patients scheduled for toncilectomia need postoperative paintreatment. Morphine has sideeffects: Nausea, vomiting, sedation and dizziness. These sideeffects are og couse unpleasent for the patient ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003122-25 | Sponsor Protocol Number: ICS-1-05 | Start Date*: 2005-11-24 |
| Sponsor Name:ANGEL LANAS | ||
| Full Title: EFECTO DEL ÁCIDO ACETILSALICÍLICO EN LA PROLIFERACIÓN Y APOPTOSIS CELULAR DEL EPITELIO METAPLÁSICO DEL ESÓFAGO DE BARRETT | ||
| Medical condition: Esófago de Barrett. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-003627-37 | Sponsor Protocol Number: IT-04-04 | Start Date*: 2006-09-22 | |||||||||||
| Sponsor Name:ALCON ITALIA | |||||||||||||
| Full Title: Hypotonic efficacy and tollerability of concomitant supply of Travoprost e Brinzolamide vs dorzolamide-timololo in fixed association in patient with glaucoma or ocular hypertension clinical study,... | |||||||||||||
| Medical condition: Patient with glaucoma or ocular hypertension bilateral non controlled | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002614-38 | Sponsor Protocol Number: HMR1964A/4002 | Start Date*: 2006-09-07 | |||||||||||
| Sponsor Name:SANOFI AVENTIS GROUPE | |||||||||||||
| Full Title: COMPARISON OF TWO THERAPEUTIC STRATEGIES FOR TREATING TYPE 2 DIABETIC PATIENTS POORLY CONTROLLED WITH BASAL INSULIN ASSOCIATED WITH ORAL ANTIDIABETIC DRUGS: 6-MONTH PROOF OF CONCEPT STUDY | |||||||||||||
| Medical condition: Type II diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001297-27 | Sponsor Protocol Number: BRN03 | Start Date*: 2005-06-08 |
| Sponsor Name:Neolab td | ||
| Full Title: Comparative Efficacy & Safety of Two Intranasal Fluticasone Propionate Formulations in Persistent Allergic Rhinitis | ||
| Medical condition: Persistent allergic rhinitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-000376-14 | Sponsor Protocol Number: CLAF237A2309 | Start Date*: 2004-05-28 | |||||||||||
| Sponsor Name:NOVARTIS FARMA | |||||||||||||
| Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, ACTIVE CONTROLLED STUDY TO COMPARE THE EFFECT OF 52 WEEKS TREATMENT WITH LAF237 50 MG BID TO METFORMIN UP TO 1000 MG BID IN DRUG NAIVE PATIENTS WITH TYPE 2 ... | |||||||||||||
| Medical condition: MONOTHERAPY TREATMENT OF PATIENTS WITH TYPE 2 DIABETES | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005363-28 | Sponsor Protocol Number: AST001 | Start Date*: 2006-07-11 |
| Sponsor Name:Ocera Therapeutics, Inc. | ||
| Full Title: A DOUBLE BLIND, RANDOMIZED, PLACEBO-CONTROLLED MULTICENTER STUDY TO ASSESS THE SAFETY AND EFFICACY OF AST-120 IN MILD TO MODERATELY ACTIVE CROHN’S PATIENTS WITH FISTULAS | ||
| Medical condition: The two main categories of inflammatory bowel disease (IBD) are ulcerative colitis and Crohn’s disease. Crohn’s disease is characterized by recurring episodes of suppurative inflammation of any par... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) CZ (Completed) BE (Completed) DE (Completed) HU (Completed) AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-003906-81 | Sponsor Protocol Number: A7-2 | Start Date*: 2005-01-14 |
| Sponsor Name:Oncology Institute of Vilnius University | ||
| Full Title: Chemoradiation with once weekly gemcitabine for invasive bladder cancer | ||
| Medical condition: Invasive transitional cell bladder cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: LT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001045-34 | Sponsor Protocol Number: ASL604LIOM02 Studio CPTTS | Start Date*: 2005-04-05 | |||||||||||
| Sponsor Name:AZIENDA USL 6 LIVORNO ZONA LIVORNESE | |||||||||||||
| Full Title: Metronomic chemiotherapic treatment WITH IRINOTECAN Cpt-11 IN PATIENTS WITH metastatic colon-rectal cancer PHARMACODYNAMIC And PHARMACOKINETIC evaluation. | |||||||||||||
| Medical condition: Colonrectal metatstatic cancer | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001065-41 | Sponsor Protocol Number: CSET 2006/1205 | Start Date*: 2007-04-30 |
| Sponsor Name:Institut Gustave Roussy | ||
| Full Title: Phase 2 single-arm studies of gemcitabine in combination with oxaliplatin in refractory and relapsed pediatric solid tumors | ||
| Medical condition: refractory or relapsing malignant pediatric solid tumors | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: DE (Completed) IT (Completed) GB (Completed) NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004442-16 | Sponsor Protocol Number: cro524 | Start Date*: 2006-11-29 | |||||||||||
| Sponsor Name:Imperial College London | |||||||||||||
| Full Title: Modulation of lung injury complicating lung resection | |||||||||||||
| Medical condition: Acute respiratory distress syndrome, Acute Lung Injury, Ventilator-Induced Lung Injury | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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