- Trials with a EudraCT protocol (44,353)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,353 result(s) found.
Displaying page 1,223 of 2,218.
EudraCT Number: 2006-002449-36 | Sponsor Protocol Number: ALGINF-2006/01 | Start Date*: 2006-10-23 | |||||||||||
Sponsor Name:Laboratorio de Aplicaciones Farmacodinámicas S.A. | |||||||||||||
Full Title: Ensayo clínico, multicéntrico, aleatorizado, simple ciego, paralelo, para evaluar la eficacia antipirética de lisinato de ibuprofeno versus ibuprofeno base en niños con procesos febriles. Multicent... | |||||||||||||
Medical condition: Procesos febriles en población infantil. Febrile processes in child population. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004369-34 | Sponsor Protocol Number: UMC-NMZ-SMA2011 | Start Date*: 2015-04-22 | ||||||||||||||||
Sponsor Name:Universtiy Medical Center Utrecht | ||||||||||||||||||
Full Title: SPACE trial SMA and Pyridostigmine in Adults and Children; Efficacy trial Phase II, mono-center, doubleblind, placebo-controlled, crossover trial to assess efficacy of pyridostigmine in patients ... | ||||||||||||||||||
Medical condition: Proximal spinal muscular atrophy (SMA) is characterized by weakness of predominantly axial and proximal muscle groups and is caused by homozygous deletion of the survival motor neuron 1 (SMN1)-gene... | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000064-21 | Sponsor Protocol Number: LPS15918 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Sanofi Aventis Groupe (SAG) | |||||||||||||
Full Title: A randomized, open-label, active comparator, 2-arm, prospective study to assess the glycosphingolipid clearance and clinical benefits of agalsidase beta (Fabrazyme®) in male patients with classic F... | |||||||||||||
Medical condition: Fabry's disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: NO (Prematurely Ended) CZ (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003230-15 | Sponsor Protocol Number: BEV-EFF | Start Date*: 2006-10-17 |
Sponsor Name:University Clinic Internal Medicine I | ||
Full Title: Phase I/II study investigating increasing doses of bevacizumab in patients with malignant effusion | ||
Medical condition: Malignant effusion in cancer patients requiring frequent centesis, at least two within six weeks | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002119-81 | Sponsor Protocol Number: MEC-2018-091 | Start Date*: 2018-09-05 |
Sponsor Name:Erasmus MC | ||
Full Title: Carriage of S. aureus and interaction with the nasal microbiome | ||
Medical condition: S. aureus carriage | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014016-35 | Sponsor Protocol Number: 2008/258 | Start Date*: 2009-09-17 | |||||||||||||||||||||
Sponsor Name:Afdeling V, Aarhus Sygehus | |||||||||||||||||||||||
Full Title: Jernsubstitution efter øvre mavetarmblødning Undersøgelse af effekten af jernbehandling peroralt (Ferro Duretter® ) eller Intravenøst (Ferinject®) i 3 måneder efter udskrivelse versus ingen jernbe... | |||||||||||||||||||||||
Medical condition: Patienter, der har haft akut øvre gastrointestinal blødning med efterfølgende endoskopisk intervention og har nedsat hæmoglobinniveau (mindre end nedre referenceinterval værdi) ved udskrivelsestids... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001812-50 | Sponsor Protocol Number: OCZ103-206 | Start Date*: 2012-09-18 | |||||||||||
Sponsor Name:Oncozyme Pharma Inc | |||||||||||||
Full Title: A Phase IIa Exploratory Study of OCZ103-OS in Combination with Platinum-Gemcitabine based Doublet First Line Therapy in Stage IV Non-Small Cell Lung Cancer (NSCLC) Patients | |||||||||||||
Medical condition: Stage IV metastatic non small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001400-11 | Sponsor Protocol Number: BBH-BDTAP-APP | Start Date*: 2013-06-04 | |||||||||||
Sponsor Name:Department of anesthesiology, Bispebjerg Hospital | |||||||||||||
Full Title: Optimal postoperative pain management by ultrasoundguided abdominal wall nerve blockade for laparoscopic surgery for acute appendicitis - a randomised controlled trial. | |||||||||||||
Medical condition: Postoperative pain following laparoscopic surgery due to acute appendicitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000985-36 | Sponsor Protocol Number: EMCAM-2011-001 | Start Date*: 2013-02-22 | |||||||||||
Sponsor Name:JOSE MANUEL GARCIA DOMINGUEZ | |||||||||||||
Full Title: Study on the Use of surface electromyography in the detection of objective differencies in patients with spasticity due to multiple sclerosis identified as "responders" and "not responders" under t... | |||||||||||||
Medical condition: Spasticity due to multiple sclerosis identified as "responders" and "not responders" under treatment with Sativex | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005571-89 | Sponsor Protocol Number: FM53 | Start Date*: 2015-06-22 | |||||||||||
Sponsor Name:Futura Medical Developments Ltd. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, home use, cross-over clinical trial of topically-applied glyceryl trinitrate (GTN) for the treatment of Erectile Dysfunction | |||||||||||||
Medical condition: This study investigates a drug intended for the treatment of male patients self-diagnosed with Erectile Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002462-24 | Sponsor Protocol Number: T4drops-01 | Start Date*: 2015-11-18 | |||||||||||
Sponsor Name:UNI-PHARMA SA | |||||||||||||
Full Title: Clinical study of the efficacy of liquid (drops) versus classic (tablets) formulations of Levothyroxine in replacement therapy of congenital hypothyroidism in infancy and childhood | |||||||||||||
Medical condition: Hypothyroidism in children. | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002230-41 | Sponsor Protocol Number: PPH-LYF02 | Start Date*: 2015-06-29 |
Sponsor Name:Landspitali University Hospital | ||
Full Title: Pharmacokinetics of Proton Pump Inhibitors in a random Icelandic Population. | ||
Medical condition: Gastro Oesophageal Reflux Disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003914-15 | Sponsor Protocol Number: Studienprotokoll/V5.1/01.12.2013 | Start Date*: 2014-06-17 |
Sponsor Name:Medizinische Universität Wien, Klinik für Innere Medizin III, Klin. Abteilung für Nephrologie und Dialyse | ||
Full Title: Continuos versus periodic intravenous iron supplementation in maintenance hemodialysis patients | ||
Medical condition: Anemia and iron deficiency in patients with end-stage renal disease on maintenance dialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011159-29 | Sponsor Protocol Number: PDA | Start Date*: 2009-06-23 |
Sponsor Name:Institut de Recerca de l?Hospital de la Santa Creu i Sant Pau | ||
Full Title: Ensayo clínico sobre la evaluación de las estrategias de tratamiento diferido con antibióticos en las infecciones respiratorias agudas no complicadas en atención primaria (Estudio PDA) | ||
Medical condition: Non-complicated acute respiratory infections | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006390-24 | Sponsor Protocol Number: DISCI-Studie | Start Date*: 2007-03-23 |
Sponsor Name:WALA Heilmittel GmbH | ||
Full Title: Prospektive, randomized, controlled, multicentre, partly double blind study to compare Disci/Rhus toxicodendron comp., placebo and waiting list in patients with chronic low back pain. | ||
Medical condition: chronic low back pain (chronic local or pseudoradiculaere low back pain due to e.g. degenerative basic illness). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005759-21 | Sponsor Protocol Number: | Start Date*: 2011-04-21 | |||||||||||
Sponsor Name:University of Oxford | |||||||||||||
Full Title: Can atorvastatin improve vascular function in women with a history preeclampsia? A Randomised, double-blinded, placebo-controlled crossover trial of atorvastatin in women with a history of preeclam... | |||||||||||||
Medical condition: Cardiovascular disease in women with a history of preeclampsia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002763-18 | Sponsor Protocol Number: HZNP-TEP-301 | Start Date*: 2018-02-22 | |||||||||||
Sponsor Name:Horizon Therapeutics USA, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Masked, Placebo-Controlled, Parallel-Group, Multicenter Study Evaluating Teprotumumab (HZN-001) Treatment in Subjects with Active Thyroid Eye Disease (OPTIC Trial) | |||||||||||||
Medical condition: Active Thyroid Eye Disease (TED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007974-39 | Sponsor Protocol Number: AIO-KRK-0207 | Start Date*: 2009-08-04 | ||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | ||||||||||||||||||
Full Title: Randomized three arm phase III trial on induction treatment with a fluoropyrimidine-, oxaliplatin- and bevacizumab-based chemotherapy for 24 weeks followed by maintenance treatment with a fluoropyr... | ||||||||||||||||||
Medical condition: Histologically confirmed and inoperable or irresectable metastatic colorectal cancer (stage IV) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001237-65 | Sponsor Protocol Number: | Start Date*: 2017-06-29 | ||||||||||||||||
Sponsor Name:Queen Mary University of London, Joint Research Management Office | ||||||||||||||||||
Full Title: Helping Pregnant smokers quit: A multi-centre RCT of electronic cigarettes and nicotine patches | ||||||||||||||||||
Medical condition: Tobacco dependence/smoking cessation | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000047-99 | Sponsor Protocol Number: MK-0476P2181V1 | Start Date*: 2007-03-06 | ||||||||||||||||||||||||||
Sponsor Name:Tari Haahtela | ||||||||||||||||||||||||||||
Full Title: Montelukast as a controller of atopic syndrome - MONTAS-study | ||||||||||||||||||||||||||||
Medical condition: Allergic symptoms (rhinitis, conjunctivits, asthma, oral symptoms and atopic eczema) caused by pollen allergy to birch or timothy. | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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