- 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 898 of 2,219.
| EudraCT Number: 2009-009596-35 | Sponsor Protocol Number: | Start Date*: 2009-03-17 |
| Sponsor Name:Queen Mary's, University of London | ||
| Full Title: Optimisation of Peri-operative Cardiovascular Management to Improve Surgical Outcome (Optimise Trial) | ||
| Medical condition: Post-operative complications in patients who undergo major surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-018218-21 | Sponsor Protocol Number: NIC-03 | Start Date*: 2010-06-02 | |||||||||||
| Sponsor Name:Menarini Ricerche S.p.A. | |||||||||||||
| Full Title: Double-blind, randomised, placebo-controlled, parallel group study to evaluate the efficacy and safety of oral administration of Nepadutant in infant colic | |||||||||||||
| Medical condition: Infant Colic | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-002437-19 | Sponsor Protocol Number: 251101 | Start Date*: 2011-10-28 | |||||||||||
| Sponsor Name:Baxter Innovations GmbH | |||||||||||||
| Full Title: BAX326 (RECOMBINANT FACTOR IX): A PHASE 2/3 PROSPECTIVE, UNCONTROLLED, MULTICENTER STUDY EVALUATING PHARMACOKINETICS, EFFICACY, SAFETY, AND IMMUNOGENICITY IN PREVIOUSLY TREATED PEDIATRIC PATIENTS W... | |||||||||||||
| Medical condition: Pediatric previously treated patients (PTPs) with severe (FIX level < 1%) or moderately severe (FIX level ≤ 2%) hemophilia B. | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001838-13 | Sponsor Protocol Number: FAB-CL-205 | Start Date*: 2009-05-05 | |||||||||||
| Sponsor Name:Amicus Therapeutics, Inc. | |||||||||||||
| Full Title: Open Label Extension Study to Evaluate the Long-term Safety Tolerability and Pharmacodynamics of AT1001 in Patients with Fabry Disease | |||||||||||||
| Medical condition: Fabry Disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003933-32 | Sponsor Protocol Number: A092358 | Start Date*: 2011-09-21 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and the University of Cambridge | |||||||||||||
| Full Title: A randomised, blind, placebo controlled crossover study of the influence of the HCN channel-blocker ivabradine on the symptoms of neuropathic pain | |||||||||||||
| Medical condition: Neuropathic Pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017480-42 | Sponsor Protocol Number: SG005 | Start Date*: 2010-03-03 |
| Sponsor Name:Synairgen Research Ltd | ||
| Full Title: A randomised, double-blind, placebo-controlled Phase II study, comparing the efficacy and safety of inhaled SNG001 to placebo administered to asthmatic subjects after the onset of a respiratory vir... | ||
| Medical condition: prevention or attenuation of asthma symptoms caused by respiratory viruses | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-000692-14 | Sponsor Protocol Number: HKO-22112010 | Start Date*: 2011-11-03 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Hannu Kokki | ||||||||||||||||||||||||||||||||||||||
| Full Title: | ||||||||||||||||||||||||||||||||||||||
| Medical condition: | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-004031-31 | Sponsor Protocol Number: RVH006 | Start Date*: 2011-11-15 | |||||||||||
| Sponsor Name:RespiVert Ltd | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, parallel group study to evaluate the safety and tolerability of treatment with repeat doses of inhaled RV568 in patients with COPD. | |||||||||||||
| Medical condition: chronic obstructive pulmonary disease (COPD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019484-10 | Sponsor Protocol Number: E7080-G000-205 | Start Date*: 2011-07-18 | ||||||||||||||||
| Sponsor Name:Eisai Ltd | ||||||||||||||||||
| Full Title: An open-label, multicenter Phase Ib/2 study of E7080 alone, and in combination with everolimus in subjects with unresectable advanced or metastatic renal cell carcinoma following one prior VEGF-tar... | ||||||||||||||||||
| Medical condition: Unresectable Advanced or Metastatic Renal Cell Carcinoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) CZ (Completed) PL (Completed) ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-024048-14 | Sponsor Protocol Number: CRO1793 | Start Date*: 2011-12-22 | ||||||||||||||||
| Sponsor Name:Imperial College London | ||||||||||||||||||
| Full Title: A randomised-controlled trial of donepezil for motor recovery in acute stroke | ||||||||||||||||||
| Medical condition: Acute stroke (ischemic and hemorrhagic strokes, starting within 4 days of onset) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-019649-24 | Sponsor Protocol Number: SM1-HT-2010 | Start Date*: 2010-06-09 | |||||||||||
| Sponsor Name:Ann Merete Møller | |||||||||||||
| Full Title: Effekten af Transversus Abdominis Plane (TAP) blok som postoperativ smertebehandling efter laparoskopisk kolonkirurgi. | |||||||||||||
| Medical condition: Postoperativ smertebehandling efter laparoskopisk kolon kirurgi hos patienter med colon cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-019973-13 | Sponsor Protocol Number: CQAX576A2209 | Start Date*: 2011-01-14 | ||||||||||||||||
| Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
| Full Title: A multi-center, randomized, double-blind, active controlled study to assess efficacy, safety and tolerability of the anti-IL13 monoclonal antibody QAX576 in the treatment of perianal fistulas in pa... | ||||||||||||||||||
| Medical condition: Treatment of perianal fistulas in patients suffering from Crohn's Disease. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| 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 | ||
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