- Trials with a EudraCT protocol (44,351)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,351 result(s) found.
Displaying page 24 of 2,218.
EudraCT Number: 2005-000192-17 | Sponsor Protocol Number: GO-80, V1 18 Mar 05 | Start Date*: 2005-05-18 |
Sponsor Name:Barts & The London NHS Trust | ||
Full Title: Gemcitabine and Oxaliplatin in the treatment of locally advanced or metastatic transitional cell carcinoma of the urinary tract in patients with impaired renal function and patients who have progr... | ||
Medical condition: Locally advanced or metastatic transitional cell carcinoma of the urinary tract | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001881-33 | Sponsor Protocol Number: AEO-2007-01 | Start Date*: 2007-05-21 |
Sponsor Name:Medicinsk gastroenterologisk afdeling, Aalborg sygehus S. | ||
Full Title: Undersøgelse af opioiders effekt på eksperimentel hyperalgesi i spiserør og hud samt på en iskæmisk muskelmodel, inklusiv et eksplorativt studie af morfins ændringer i hjernens smerte processering. | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004834-33 | Sponsor Protocol Number: ROB 803-09-002 | Start Date*: 2007-07-05 | |||||||||||
Sponsor Name:OxyPharma AB | |||||||||||||
Full Title: A Phase II, Randomised, Double-blind, International, Multicentre, Placebo-controlled, Dose-ranging, Parallel-group Study to Evaluate the Efficacy and Safety of Orally Administered Rob 803 when Adde... | |||||||||||||
Medical condition: Rheumatiod Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) LV (Completed) GB (Completed) BE (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004840-21 | Sponsor Protocol Number: RISED_C_00935 | Start Date*: 2007-04-23 | |||||||||||
Sponsor Name:sanofi-aventis Netherlands B.V. | |||||||||||||
Full Title: Bone Histomorphometry, Microarchitecture and Matrix Structure and Properties in Patients Receiving Long-term Risedronate Treatment | |||||||||||||
Medical condition: The objective of this study is to collect data on bone histomorphometry, architecture, turnover and material properties from iliac crest biopsies taken from postmenopausal women after > 5 year rise... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004849-42 | Sponsor Protocol Number: 88/2006/O/Sper | Start Date*: 2006-11-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Cetuximab + Irinotecano vs chemoterapia standard nel carcinoma colo-rettale avanzato pretrattato non resecabile esprimente EGFR | |||||||||||||
Medical condition: carcinoma colo-rettale avanzato | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002002-19 | Sponsor Protocol Number: MODAGE MO 169 | Start Date*: 2008-06-11 |
Sponsor Name:BIOCODEX | ||
Full Title: Effets du moclobémide sur le profil d'activation cérébrale de patients dépressifs âgés lors de tâches cognitives et émotionnelles, en référence à des sujets témoins. Etude ouverte, multicentrique, ... | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005033-11 | Sponsor Protocol Number: SRx-501-01 | Start Date*: 2008-03-27 |
Sponsor Name:CombinatoRx, Inc | ||
Full Title: A Comparison Of The Safety And Bioavailability Of Modified-Release Formulations Of Levodopa-Carbidopa In Subjects With Parkinson’s Disease | ||
Medical condition: Patients with Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000905-12 | Sponsor Protocol Number: CCD-0802-PR-0029 | Start Date*: 2008-08-20 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: A single dose, randomized, double blind, double dummy, placebo controlled, three-period crossover clinical study, comparing the onset of relief from methacholine induced bronchoconstriction with ... | |||||||||||||
Medical condition: Ashtma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000928-71 | Sponsor Protocol Number: GOIRC02/2008-TWIST | Start Date*: 2008-11-14 | |||||||||||||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA | |||||||||||||||||||||||
Full Title: TWIST. RANDOMIZED PROSPECTIVE PHASE II STUDY OF TEMSIROLIMUS WITH OR WITHOUT LOW-DOSE INTERFERON ALPHA IN METASTATIC NON-CLEAR RENAL CELL CARCINOMA: GOIRC STUDY 02/2008 | |||||||||||||||||||||||
Medical condition: Patients with advanced non-clear Cell Renal Carcinoma. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000942-29 | Sponsor Protocol Number: 6520-0650-13 | Start Date*: 2008-06-23 |
Sponsor Name:Medice Arnzneimittel Pütter GmbH & Co. KG | ||
Full Title: Quality assurance of methylphenidate administration in adults with ADHS | ||
Medical condition: Aufmerksamkeitsdefizit/Hyperaktivitätsstörungen (ADHS) bei Erwachsenen | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-000259-33 | Sponsor Protocol Number: 06-AnIt-06 | Start Date*: 2007-08-16 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Department of Anesthesiology and Intensive Care, University Hospital Münster | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Perioperative protective effects of lidocaine - clinical study on the route and timing of administration | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: patients, scheduled for major elective colorectal surgery | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000271-42 | Sponsor Protocol Number: 11012007 | Start Date*: 2007-05-08 | |||||||||||
Sponsor Name:Matti Eskelinen | |||||||||||||
Full Title: OKSIKODONIN ANALGEETTINEN PITOISUUS PLASMASSA YHDESSÄ PARASETAMOLIN 1g TAI 2g IV KANSSA ANNETTUNA MAHAKIRURGISILLA POTILAILLA | |||||||||||||
Medical condition: Tutkimukseen otetaan 24 sappileikkaukseen tulevaa perustervettä aikuispotilasta. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002542-38 | Sponsor Protocol Number: CAEB071A2210 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double blind, placebo controlled, parallel group design study to explore the efficacy, safety and tolerability of AEB071 in patients with active, moderate to severe ulcerative colitis. | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005254-68 | Sponsor Protocol Number: GEL/TAMO-2006 | Start Date*: 2007-04-13 |
Sponsor Name:GEL/TAMO (Cooperative Spanish Group of Lymphoma/Autologous bone marrow transplant). | ||
Full Title: Treatment with R-MegaCHOP and early rescue with R-IFE and autologous stem cells transplant (ASCT) according response measured by positron emission tomography (PET) in patients with diffuse large B-... | ||
Medical condition: Diffuse Large B-Cell Lymphoma (DLBCL) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005152-16 | Sponsor Protocol Number: BV-2007/04 | Start Date*: 2008-10-07 | |||||||||||
Sponsor Name:OM Pharma SA | |||||||||||||
Full Title: Multicentre, randomised, double-blind, placebo-controlled study of the efficacy and safety of Broncho-Vaxom in adults suffering from chronic rhinosinusitis | |||||||||||||
Medical condition: Chronic rhinosinusitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005163-94 | Sponsor Protocol Number: BAY81-8781/12946 | Start Date*: 2010-10-08 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A prospective, randomized, verum controlled, open label, parallel group multi-center phase III clinical trial to demonstrate the superiority of 500 or 250 mg Aspirin® i.v. (BAY 81-8781) treatment v... | |||||||||||||
Medical condition: Acute coronary syndrome (ACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005164-27 | Sponsor Protocol Number: 260981 | Start Date*: 2008-02-22 |
Sponsor Name:research office urology VUmc | ||
Full Title: Botulinum toxin A intravesical injections in the treatment of Bladder Pain Syndrome/ Interstitial Cystitis | ||
Medical condition: Interstitial Cystitis (IC) is a syndrome characterized by bladder pain associated with urgency, frequency, nocturia, dysuria and sterile urine. The patho-physiology remains largely unclear. No univ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005169-36 | Sponsor Protocol Number: NKV110721 | Start Date*: 2008-02-07 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: NKV110721, A Study of Single Dose Intravenous Casopitant in Combination with Ondansetron and Dexamethasone for the Prevention of Oxaliplatin-Induced Nausea and Vomiting | ||
Medical condition: Prevention of nausea and vomiting due to first cycle of oxaliplatin based chemotherapy in patients with colorectal cancer receiving a combination with 5-fluorouracil and leucovorin, or in combinati... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) CZ (Completed) DE (Completed) HU (Completed) IT (Completed) SK (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002494-75 | Sponsor Protocol Number: CL3-12911-018 | Start Date*: 2006-04-26 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: The efficacy and safety of two doses of strontium ranelate (1g and 2g per day) versus placebo administered orally for 3 years in the treatment of knee osteoarthritis. A prospective multicentre, int... | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) BE (Completed) GB (Completed) ES (Completed) IT (Completed) DK (Completed) PT (Completed) LT (Completed) EE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000971-41 | Sponsor Protocol Number: GGCP032/07 | Start Date*: 2007-07-03 | ||||||||||||||||
Sponsor Name:Grupo Gallego de Cáncer de Pulmón | ||||||||||||||||||
Full Title: Estudio fase II de bevacizumab en combinación con vinorelbina y cisplatino, como tratamiento de primera línea de pacientes con cáncer de pulmón no microcítico,no epidermoide, estadio IIIB con derra... | ||||||||||||||||||
Medical condition: Cáncer de pulmón no microcítico(CPNM), no epidermoide, estadio IIIB con derrame pleural o IV / on-small cell, non-squamous lung cancer, stage IIIb with pleural effusion or stage IV. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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