- 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 33 of 2,219.
| EudraCT Number: 2007-004980-23 | Sponsor Protocol Number: P05134 | Start Date*: 2008-05-05 | |||||||||||
| Sponsor Name:Schering-Plough Farma, Lda. | |||||||||||||
| Full Title: Double-Blind evaluation of the safety and efficacy of Quadriderme cream (betamethasone dipropionate, clotrimazole and gentamicin sulphate ) compare with betamethasone dipropionate combined with gen... | |||||||||||||
| Medical condition: Impetiginous Eczema | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004985-41 | Sponsor Protocol Number: DYSK-PD-2007 | Start Date*: 2007-11-29 |
| Sponsor Name:Department of Neuroscience, neurology | ||
| Full Title: Different dyskinesias in Parkinson's disease and their relation to levodopa pharmacokinetics | ||
| Medical condition: Parkinson's disease, G20.9. Different dyskinesias related to advanced Parkinson's disease will be investigated. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-004994-25 | Sponsor Protocol Number: CSMS995A2101 | Start Date*: 2008-02-04 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A multi-center, randomized, double-blind, placebo-controlled, crossover study in women with irritable bowel syndrome to evaluate feasibility and reproducibility of barostat assessments of colorecta... | |||||||||||||
| Medical condition: Irritable Bowel Syndrom | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002335-32 | Sponsor Protocol Number: AN08/8505 | Start Date*: 2008-11-28 |
| Sponsor Name:The University of Leeds | ||
| Full Title: Does concentration affect the ED50 of bupivacaine for supraclavicular brachial plxus block? | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-002343-16 | Sponsor Protocol Number: 1014/05 | Start Date*: 2006-01-05 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Postoperative nausea and vomiting: acupuncture effect on postoperative prevention | |||||||||||||
| Medical condition: Postoperative nausea and vomiting laparoscopic cholecistectomy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-000526-48 | Sponsor Protocol Number: A.S.T.R.A. | Start Date*: 2007-03-06 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
| Full Title: Randomized, monocentric trial on sintoms, adherence,toxicity of alternate antiretrovirale regimen | |||||||||||||
| Medical condition: PT HIV-1 positive and naive to antiretroviral drug | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001465-14 | Sponsor Protocol Number: CSLCT-NHF-06-30 | Start Date*: 2007-05-17 |
| Sponsor Name:CSL Limited | ||
| Full Title: A Single Centre, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira Vaccine in Healthy Adults aged ≥ 18 to < 60 years and in Healthy Older Adults aged ≥ 60 years for the 2007/2008... | ||
| Medical condition: Prophylaxis of Influenza | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-001187-78 | Sponsor Protocol Number: 112897 | Start Date*: 2008-01-02 | |||||||||||
| Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: The 3Mg Trial: A randomised controlled trial of intravenous or nebulised magnesium sulphate versus standard therapy for acute severe asthma | |||||||||||||
| Medical condition: Acute severe asthma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001206-24 | Sponsor Protocol Number: 16901 | Start Date*: 2007-07-31 |
| Sponsor Name:UMCG | ||
| Full Title: Effect of selective COX-2 inhibition on neuroinflammation in Parkinson's disease | ||
| Medical condition: Parkinson's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-002109-32 | Sponsor Protocol Number: CORL2007 | Start Date*: 2007-05-10 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
| Full Title: USE OF FENOLDOPAM TO IMPROVE GLOMERULAR FILTRATION RATE IN EARLY RENAL DYSFUNCTION AFTER LIVER TRANSPLANTATION | |||||||||||||
| Medical condition: Adult liver transplanted patients age > 18 years , with pre-transplantation normal renal function creatinine clearance 1ml/kg/min | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002120-14 | Sponsor Protocol Number: 3074K4-2207-WW | Start Date*: 2008-10-29 | |||||||||||||||||||||
| Sponsor Name:Wyeth Research Division of Wyeth Pharmaceutical Inc. | |||||||||||||||||||||||
| Full Title: A Multicenter, Open-Label, Ascending Multiple-Dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age With Selected Serious Infections | |||||||||||||||||||||||
| Medical condition: Complicated intra-abdominal infections (cIAI), complicated skin and skin structure infections (cSSSI), community-acquired pneumonia (CAP). | |||||||||||||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) GB (Completed) Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2008-001160-36 | Sponsor Protocol Number: 2008-1 | Start Date*: 2009-06-04 | ||||||||||||||||
| Sponsor Name:Imperial College London | ||||||||||||||||||
| Full Title: A trial of Guanfacine, an alpha 2 adrenergic agonist, for Spatial Neglect and Impaired Vigilance following Stroke and Focal Brain Damage | ||||||||||||||||||
| Medical condition: Spatial Neglect following Hemispheric stroke and focal brain injury | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-006405-17 | Sponsor Protocol Number: FDM-study | Start Date*: 2009-02-25 | |||||||||||
| Sponsor Name:Kuopio University Hospital | |||||||||||||
| Full Title: Finnish Dyspepsia Management -study | |||||||||||||
| Medical condition: Tutkimukseen rekrytoidaan n. 400 dyspepsiaoireiden vuoksi erikoissairaanhoitoon lähetettyä alle 60-vuotiasta potilasta, joiden vaiva tutkimusten jälkeen todetaan toiminnalliseksi. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004526-90 | Sponsor Protocol Number: TaxErb-1 | Start Date*: 2007-01-30 | |||||||||||
| Sponsor Name:Klinik Löwenstein gGmbH | |||||||||||||
| Full Title: TaxErb-Protokoll; Docetaxel-Carboplatin Chemotherapie in Kombination mit Cetuximab bei Patienten mit local fortgeschrittenem oder metastasiertem, nicht-kleinzelligem Bronchial-Karzinom (NSCLC)-ein ... | |||||||||||||
| Medical condition: Patients with advanced or metastatic non-small cell lung cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000569-13 | Sponsor Protocol Number: EMR 64300-608 | Start Date*: 2006-04-21 |
| Sponsor Name:Cardioangiologisches Centrum Bethanien | ||
| Full Title: Influence on the coronary Microcirculation and on myocArdial perfusion Reserve of Niaspan given IN addition to simvastatin in diabEtic patients | ||
| Medical condition: Diabetic patients at high risk for CVD | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-000571-15 | Sponsor Protocol Number: 101-PG-COM-143 | Start Date*: 2007-07-13 | |||||||||||
| Sponsor Name:Laboratorios LETI S.L. | |||||||||||||
| Full Title: Extracto alergénico despigmentado polimerizado de Dermatophagoides pteronyssinus como tratamiento antiasmático en niños con asma leve alérgicos a ácaros. | |||||||||||||
| Medical condition: Asma leve por alergia a ácaros | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001984-53 | Sponsor Protocol Number: ETHIG II | Start Date*: 2006-10-11 | |||||||||||
| Sponsor Name:Friedrich-Schiller-Universität Jena | |||||||||||||
| Full Title: Effectiveness of Dalteparin Therapy as Intervention in recurrent pregnancy loss | |||||||||||||
| Medical condition: Pregnant women with a history of recurrent pregnancy loss, defined as: - 2 or more early (< 12 weeks of gestation) pregnancy losses or - 1 or more late (> 12 weeks of gestation) pregnancy loss | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001816-22 | Sponsor Protocol Number: V150960 | Start Date*: 2007-10-19 | |||||||||||
| Sponsor Name:Anne Ristikankare | |||||||||||||
| Full Title: Vasopressiinin vaikutus munuaisten toimintaan sydänleikkauksen jälkeisessä vasodilatoivassa shokissa | |||||||||||||
| Medical condition: sydänleikkauspotilaita, joilla on perfuusion jälkeinen vasodilatoiva shokki | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-002791-18 | Sponsor Protocol Number: 0476-302 | Start Date*: 2006-09-28 | |||||||||||
| Sponsor Name:Suomen MSD Oy | |||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Double-Dummy, Parallel-Group Study Evaluating the Effects of 2 Different Regimens of Montelukast (Daily Dosing and Intermittent, Episode-Driven Dosing) Comp... | |||||||||||||
| Medical condition: episodic or intermittent asthma | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DK (Completed) DE (Completed) IT (Completed) LT (Completed) FR (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002793-21 | Sponsor Protocol Number: Lactest2-06 | Start Date*: 2006-11-14 |
| Sponsor Name:Lactest S.L. | ||
| Full Title: “ Ensayo Clinico para la evaluación no invasiva de la actividad lactasa intesttinal in vivo, mediante la administracción oral de 4-Galactosil-xilosa en sujetos con clinica sugerente de intolerancia... | ||
| Medical condition: Diagnostico no invasivo de la deficiencia de lactasa intestinal | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
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