- Trials with a EudraCT protocol (26,267)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9,945)
26,267 result(s) found for: NA.
Displaying page 96 of 1,314.
| EudraCT Number: 2007-006206-24 | Sponsor Protocol Number: Aivoverenvuotopotilaan tromboosipro | Start Date*: 2008-12-17 | |||||||||||
| Sponsor Name:Hillbom Matti OYS/neurologian klinikka | |||||||||||||
| Full Title: A blind randomized trial to compare the efficacy of intermittent pneumatic compression (IPC) with and without early anticoagulant treatment for prevention of venous thromboembolism (VTE) in patient... | |||||||||||||
| Medical condition: Spontaani aivoverenvuoto | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019135-35 | Sponsor Protocol Number: PillCam2010 | Start Date*: 2010-06-11 | |||||||||||
| Sponsor Name:Dr. Enrique | |||||||||||||
| Full Title: Evaluación de la limpieza intestinal en un día para la colonoscopia con cápsula colónica: estudio piloto | |||||||||||||
| Medical condition: Detección de Cancer colorrectal | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-002170-34 | Sponsor Protocol Number: 2004-002170-34 | Start Date*: 2006-03-29 |
| Sponsor Name:Cambridge University Hospital (Addenbrookes Hospital) | ||
| Full Title: "Ensayo clínico controlado randomizado sobre el tratamiento precoz con insulina en recién nacidos de muy bajo peso" | ||
| Medical condition: Very low birth weight infants requiring intensive care have relative insulin deficiency often leading to hyperglycaemia during the first week of life. There is increasing evidence that the early po... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004158-10 | Sponsor Protocol Number: ALMED-07-C2-012 | Start Date*: 2008-04-17 |
| Sponsor Name:AIR LIQUIDE | ||
| Full Title: A single site, exploratory, phase I / II, randomised trial comparing the effect of Helium/Oxygen mixtures (He/O2 78:22 and He/O2 65:35) to medical air on pulmonary function in moderate / severe ast... | ||
| Medical condition: - healthy volunteers, - moderate and severe persistent asthmatic patients, - moderate and severe COPD patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004528-19 | Sponsor Protocol Number: I001PS0807_1 | Start Date*: 2008-01-11 |
| Sponsor Name:University of Wuerzburg | ||
| Full Title: Electrophysiological measurement of anterior cingulate cortex (ACC) function in schizophrenic patients treated with Seroquel® or Fluanxol® | ||
| Medical condition: schizophrenia (295.10, 295.20, 295.30, 295.90 according to Diagnostic and Statistical Manual of Mental Disorders- Fourth Edition (DSM-IV) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-003734-34 | Sponsor Protocol Number: BT0800BEL001 | Start Date*: 2005-03-03 |
| Sponsor Name:Barrier Therapeutics nv | ||
| Full Title: A one-weel, randomized, double-blind, placebo-controlled pilot trial to evaluate oral R129160 (60 mg b.i.d.) on the alleviation of itch in atopic dermatitis patients | ||
| Medical condition: Atopic Dermatitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-011008-43 | Sponsor Protocol Number: CRAD001AIT16 - EVERHEART | Start Date*: 2009-06-24 | |||||||||||
| Sponsor Name:NOVARTIS FARMA | |||||||||||||
| Full Title: Early vs.delayed EVERolimus in de novo HEART transplant recipients: optimozation of the safety/efficacy profile (EVERHEART Study) | |||||||||||||
| Medical condition: de novo heart transplant patients | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000103-34 | Sponsor Protocol Number: CL2-16257-062 | Start Date*: 2005-07-13 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier [...] | |||||||||||||
| Full Title: Evaluation of the effects of 3 successive oral dosages (2.5; 5; 7.5 mg b.i.d.) of ivabradine in patients with stable moderate to severe systolic chronic heart failure treated with beta-blockers. A ... | |||||||||||||
| Medical condition: Chronic systolic heart failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000497-50 | Sponsor Protocol Number: 11051 | Start Date*: 2005-11-21 | |||||||||||
| Sponsor Name:H. Lundbeck A/S | |||||||||||||
| Full Title: An open-label safety study of bifeprunox investigating flexible doses of 20, 30, or 40mg/day in patients with schizophrenia who have completed studies 10206 or 10265 | |||||||||||||
| Medical condition: male and female patients with schizophrenia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002136-25 | Sponsor Protocol Number: CLAF237A2309E1 | Start Date*: 2005-04-07 |
| Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
| Full Title: A 52-week extension to 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 naïv... | ||
| Medical condition: Type II Diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-005925-12 | Sponsor Protocol Number: polyoma IFB 29 | Start Date*: 2011-01-20 |
| Sponsor Name:Medizinische Hochschule Hannover | ||
| Full Title: Polyomavirus BK nephropathy after renal transplantation: Randomized clinical trial to demonstrate that switching to mTOR inhibitor is more effective than a reduction of immunosuppressive therapy | ||
| Medical condition: Polyoma BK-virus nephropathy is a viral complication after renal transplantation attacking up to 10% of renal transplants and causing transplant failure in 45% of cases. No virustatic treatment exi... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000934-19 | Sponsor Protocol Number: 2005-130 | Start Date*: 2005-05-19 |
| Sponsor Name:Neurologisk Afdeling Århus Universitetshospital | ||
| Full Title: Undersøgelse af subcutan immunglobulin behandling af patienter med multifokal motorisk neuropati | ||
| Medical condition: Multifokal motor neuropathy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004617-15 | Sponsor Protocol Number: ESPEKLILU05 rev. | Start Date*: 2006-07-06 |
| Sponsor Name:Klinik für Anästhesiologie und Operative Intensivmedizin Klinikum Ludwigshafen | ||
| Full Title: „Einsatz des Beta-Blockers Esmolol in Kombination mit dem Phosphodiesterase-III-Hemmer Enoximon im Vergleich zur alleinigen Gabe von Esmolol zur Optimierung der Hämodynamik bei Patienten mit korona... | ||
| Medical condition: In einer prospektiven, monozentrischen, investigator-initiierten, randomisierten klinischen Prüfung sollen Patienten mit vorbestehender koronarer Herzkrankheit, die sich einem großen, elektiven all... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004837-16 | Sponsor Protocol Number: CRAD001C2454 | Start Date*: 2006-10-04 |
| Sponsor Name:Novartis Pharma GmbH | ||
| Full Title: Multicenter, single-arm, two-stage phase II trial of RAD001 (everolismus) with Glivec® in Glivec®-resistant patients with progressive GIST | ||
| Medical condition: gastrointestinal stromal tumors (GIST) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000051-10 | Sponsor Protocol Number: A091200 | Start Date*: 2008-05-19 |
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | ||
| Full Title: 11C metomidate PET scanning for Conn's syndrome | ||
| Medical condition: Primary hyperaldosteronism - Conn's syndrome and bilateral adrenal hyperplasia. Imaging of adrenal lesions using 11C-metomidate PET. Pre-suppression with dexamethasone and/or fludrocortisone to opt... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001046-13 | Sponsor Protocol Number: BUC-58/BIO | Start Date*: 2006-04-19 |
| Sponsor Name:Dr. Falk Pharma GmbH | ||
| Full Title: Pharmacokinetic interaction study between budesonide and metronidazole in healthy volunteers | ||
| Medical condition: Healthy male volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000506-21 | Sponsor Protocol Number: Chumbley1 | Start Date*: 2011-06-21 |
| Sponsor Name:Imperial College Healthcare NHS Trust | ||
| Full Title: A double-blind, randomised placebo-controlled trial to determine whether low-dose intravenous ketamine peri-operatively can prevent chronic post-surgical pain, in patients undergoing thoracotomy or... | ||
| Medical condition: Chronic post-surgical pain | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003901-10 | Sponsor Protocol Number: 250317BS | Start Date*: 2006-12-06 |
| Sponsor Name:Neosil Inc. | ||
| Full Title: A randomized, placebo controlled, double-blind study to evaluate the efficacy of topical formulations in male subjects with androgenetic alopecia | ||
| Medical condition: The study will be performed in male subjects with Norwood/Hamilton grades III - IV, androgenetic alopecia. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001097-27 | Sponsor Protocol Number: MONO-01 | Start Date*: 2005-09-29 |
| Sponsor Name:Bio-Gels Pharmaceuticals | ||
| Full Title: A Study of the Clinical Activity of Monocaprin/Doxycycline Gel on Cold Sores | ||
| Medical condition: Herpes simplex virus (HSV) has plagued mankind worldwide for thousands of years. Once HSV enters the body, it penetrates vulnerable cells in the lower layers of human skin tissue and replicates its... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IS (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006369-10 | Sponsor Protocol Number: BTT-gpASIT003 | Start Date*: 2009-01-22 |
| Sponsor Name:BioTech Tools S.A. | ||
| Full Title: Preliminary assessment of the clinical tolerability, safety and immunogenicity of three different doses of grass pollen-derived peptides for oral use in antigen-specific immunotherapy of seasonal a... | ||
| Medical condition: seasonal allergic rhinoconjunctivitis | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
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