- Trials with a EudraCT protocol (26,035)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
26,035 result(s) found.
Displaying page 714 of 1,302.
EudraCT Number: 2010-022319-20 | Sponsor Protocol Number: 24638418 | Start Date*: 2011-10-13 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: The effect of antidepressant therapy on quality of life, physical and menthal health and cortisole metabolism in PCOS. | |||||||||||||
Medical condition: Polycystic Ovary Syndrome, PCOS, is the most common endocrine disorder in fertile women. Insuliresistance, hirsutism, hyperandrogenemia, adipositas, high cortisole levels and infertility are freque... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002773-39 | Sponsor Protocol Number: 82828282 | Start Date*: 2011-09-28 |
Sponsor Name:Universitetssjukhuset Örebro | ||
Full Title: | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016628-29 | Sponsor Protocol Number: HLPTRA-2009-01 | Start Date*: 2011-06-28 | |||||||||||
Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario La Paz (FIBHULP) | |||||||||||||
Full Title: Ensayo clínico comparativo para la reparación de defectos condrales de rodilla: trasplante autólogo de condrocitos cultivados vs. células troncales mesenquimales autólogas procedentes de tejido adi... | |||||||||||||
Medical condition: Pacientes con lesiones condrales de rodilla | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001526-19 | Sponsor Protocol Number: BO27798 | Start Date*: 2011-12-28 | ||||||||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: A randomized, open-label, multicenter Phase IIIb study comparing two trastuzumab dosing regimens, each in combination with cisplatin/ capecitabine chemotherapy, as first-line therapy in patients wi... | ||||||||||||||||||
Medical condition: Metastatic HER2-positive adenocarcinoma of the stomach or gastro-esophageal junction. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) PT (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001841-34 | Sponsor Protocol Number: PLUTO2011 | Start Date*: 2012-01-12 | |||||||||||||||||||||
Sponsor Name:NHS Greater Glasgow Health Board [...] | |||||||||||||||||||||||
Full Title: A Randomised Phase II study investigating pazopanib vs weekly paclitaxel in relapsed or progressive Transitional Cell Carcinoma (TCC) of the urothelium. | |||||||||||||||||||||||
Medical condition: Relapsed or progressive Transitional Cell Carcinoma (TCC) of the urothelium | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000762-35 | Sponsor Protocol Number: ID_2882 | Start Date*: 2011-11-18 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: EFFECTS OF THE VITAMIN D ADMINISTRATION ON RESPIRATORY FUNCTIONS IN PAEDIATRIC PATIENTS SUFFERING FROM EFFORT ASTHMA | |||||||||||||
Medical condition: paediatric patients suffering from effort asthma | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005806-32 | Sponsor Protocol Number: SAN-LTM-001 | Start Date*: 2011-12-21 | |||||||||||
Sponsor Name:ikfe GmbH | |||||||||||||
Full Title: Clinical Study to Collect Clinical Data Sets for Development of Insulin Glargine Titration Algorithms | |||||||||||||
Medical condition: Type 2 diabetes mellitus receiving BOT Therapy or insulin therapy only | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005059-15 | Sponsor Protocol Number: buspironeesostim2011 | Start Date*: 2012-02-03 |
Sponsor Name:uzleuven | ||
Full Title: The effect of Buspirone on esophageal sensitivity in healthy volunteers: a randomized, double-blind, placebo-controlled, single-dosing study. | ||
Medical condition: altered esophageal sensitivity, gastro-esophageal reflux disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003570-89 | Sponsor Protocol Number: 37559 | Start Date*: 2011-12-02 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: The effect of interferon beta-1a treatment on functional adaptation in Multiple Sclerosis (MS) | |||||||||||||
Medical condition: Multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004030-33 | Sponsor Protocol Number: RBHP2011PICKERING3 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:CHU de Clermont-Ferrand | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004910-41 | Sponsor Protocol Number: WellmuneElderlyStudy1.1 | Start Date*: 2011-12-30 |
Sponsor Name:University of Southampton | ||
Full Title: A Randomised Controlled Trial to assess a food supplement (baker’s yeast extract) to support immune function and prevent cold and flu symptoms in a 50 to 70 year old population | ||
Medical condition: We aim to assess the number and severity of Upper Respiratory Tract Infection(URTI)Symptoms reported by participants over a 90 day period commencing in January 2012 in 100 healthy 50-70 year olds p... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004497-28 | Sponsor Protocol Number: 0028022 | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:Orion Pharma | |||||||||||||
Full Title: A RANDOMISED, MULTICENTRE, TWO-ARM, PARALLEL GROUP, DOUBLE-BLIND, PLACEBO-CONTROLLED, COMPARATIVE EFFICACY AND SAFETY CLINICAL STUDY OF IBUPROFEN 5% ROLL-ON GEL IN ADULT HUMAN PATIENTS WITH PAIN RE... | |||||||||||||
Medical condition: Pain related to uncomplicaated ankle injuries. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000592-24 | Sponsor Protocol Number: PTH2008002 | Start Date*: 2008-08-11 | |||||||||||
Sponsor Name:Berufsgenossenschaftliche Unfallklinik | |||||||||||||
Full Title: A Randomized Open Clinical Study of Daily Subcutaneous Parathyroid Hormone (1-34) / Teriparatide Injection on the Consolidation of Regenerated Bone Formed after Distraction Osteogenesis. | |||||||||||||
Medical condition: Patients with tibial bone defects due to resection after osteomyelitis who are undergoing bone segment transport | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003496-11 | Sponsor Protocol Number: EN3348-303 | Start Date*: 2012-02-08 | |||||||||||
Sponsor Name:Endo Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Active-Controlled, Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of EN3348 (MCC) as Compared with Mitomycin C in the Intravesical Treatment of Subjects wi... | |||||||||||||
Medical condition: BCG Recurrent or Refractory Non-Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021437-30 | Sponsor Protocol Number: PAISII-V01 | Start Date*: 2011-02-04 | |||||||||||
Sponsor Name:ErasmusMC | |||||||||||||
Full Title: Paracetamol (Acetaminophen) in Stroke 2 (PAIS 2): A randomized, placebo-controlled clinical trial of high-dose paracetamol in patients with acute stroke and a body temperature of 36.5°C or above | |||||||||||||
Medical condition: acute stroke (cerebral infarction or intracrebral hemorrhage) and a body temperature of 36.5 degrees or above. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000241-21 | Sponsor Protocol Number: BEL114870 | Start Date*: 2011-06-23 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A clinical and mechanistic proof of efficacy study with belimumab in chronic immune thrombocytopenia (ITP) patients | |||||||||||||
Medical condition: Chronic Immune Thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006087-49 | Sponsor Protocol Number: MEK115306 | Start Date*: 2012-04-13 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Phase III, randomized, double-blinded study comparing the combination of the BRAF inhibitor, dabrafenib and the MEK inhibitor, trametinib to dabrafenib and placebo as first-line therapy in subjec... | |||||||||||||
Medical condition: Cutaneous melanoma - aggressive form of skin cancers. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) ES (Completed) GB (Completed) NL (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002931-25 | Sponsor Protocol Number: GS-US-259-0131 | Start Date*: 2012-02-28 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Ranolazine Monotherapy in Subjects with Type 2 Diabetes Mellitus | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) PL (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001345-32 | Sponsor Protocol Number: P07755 | Start Date*: 2012-03-30 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp, a Subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 3, Safety and Efficacy Study of Boceprevir/Peginterferon Alfa-2a/ribavirin in Chronic HCV Genotype 1 IL28B CC Subjects | |||||||||||||
Medical condition: Hepatitis C | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) ES (Completed) CZ (Completed) SE (Completed) AT (Completed) BE (Completed) DE (Completed) GB (Completed) PL (Completed) LT (Prematurely Ended) EE (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002035-26 | Sponsor Protocol Number: 115411 | Start Date*: 2011-10-21 | |||||||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||||||||||||
Full Title: A Phase IIIb observer-blind, randomized, multicentre primary immunization study to evaluate the immunogenicity and safety of GSK Biologicals’ HPV-16/18 L1 VLP AS04 vaccine and Merck's Quadrivalent ... | |||||||||||||||||||||||
Medical condition: Cervarix is indicated in females from 10 years of age onwards for the prevention of persistent infection, premalignant cervical lesions and cervical cancer (squamous-cell carcinoma and adenocarcino... | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) SE (Completed) | |||||||||||||||||||||||
Trial results: View results |
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