- Trials with a EudraCT protocol (11,933)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11,933 result(s) found for: II.
Displaying page 276 of 597.
| EudraCT Number: 2008-001004-22 | Sponsor Protocol Number: CRH 06/374/M | Start Date*: 2008-07-09 | |||||||||||
| Sponsor Name:Centre René Huguenin | |||||||||||||
| Full Title: A multicentre phase II trial to determine the efficacy of the anti-tyrosine kinase sunitinib (SUTENT®) as second line therapy in patients with transitional cell carcinoma (TCC) of the urothelium wh... | |||||||||||||
| Medical condition: Histologically proven advanced TCC (transitional cell carcinoma) of the urothelium | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-006097-10 | Sponsor Protocol Number: SPOT 1.9-2005 | Start Date*: 2006-09-25 |
| Sponsor Name:Universitätsklinikum Essen | ||
| Full Title: Pilot study of dose-escalated radiotherapy with PET/CT based treatment planning in combination with induction and concurrent chemotherapy in locally advanced (uT3/T4) squamous cell cancer of the es... | ||
| Medical condition: Phase II study of dose-intensified radiation therapy based on PET/CT-Planning in combination with induction- and concurrent chemotherapy in locally advanced squamous cell carcinomas (uT3/T4) of the... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Restarted) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003790-41 | Sponsor Protocol Number: JAN12006-01 | Start Date*: 2015-05-11 |
| Sponsor Name:Spherium Biomed | ||
| Full Title: Randomised, double-blinded, placebo and active comparator controlled exploratory clinical trial to assess the efficacy and safety of a triple combination of Ibuprofen, magnesium and ascorbic acid ... | ||
| Medical condition: Temporomandibular joint dysfunction syndrome. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002321-20 | Sponsor Protocol Number: HIDRA04 | Start Date*: 2015-09-01 | |||||||||||
| Sponsor Name:Hellenic Institute for the Study of Sepsis | |||||||||||||
| Full Title: A DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED CLINICAL TRIAL OF THE SAFETY AND EFFICACY OF MABp1, A HUMAN ANTIBODY TARGETING INTERLEUKIN-1ALPHA, IN PATIENTS WITH HIDRADENITIS SUPPURATIVA | |||||||||||||
| Medical condition: HIDRADENITIS SUPPURATIVA/ACNE INVERSA | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000269-27 | Sponsor Protocol Number: DSCK101 | Start Date*: 2014-11-06 |
| Sponsor Name:German Foundation for Chronically Ill | ||
| Full Title: Efficacy and tolerance of Beta Blocker and Procoralan uptitration in chronic heart failure patients under telemedical control: „70 bpm on day 28“ | ||
| Medical condition: Patients with chronic heart failure and resting heart rate of ≥ 75 bmp | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-005052-25 | Sponsor Protocol Number: AOP00101 | Start Date*: 2015-06-29 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||
| Full Title: Total versus corrected body weight for dosage of sugammadex in morbidly obese patients. | |||||||||||||
| Medical condition: Reversal of rocuronium-induced neuromuscular blockade | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002395-24 | Sponsor Protocol Number: PM60184-B-001-15 | Start Date*: 2015-12-09 | |||||||||||
| Sponsor Name:Pharma Mar, S.A. , Sociedad Unipersonal | |||||||||||||
| Full Title: Phase II, Open-Label, Randomized, Controlled Study of PM060184 in Advanced, Hormone Receptor Positive, HER2 negative Breast Cancer Patients in Third or Fourth Line Setting. | |||||||||||||
| Medical condition: Breast Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004015-49 | Sponsor Protocol Number: FLU010 | Start Date*: 2019-03-14 | |||||||||||
| Sponsor Name:Vaccitech Ltd | |||||||||||||
| Full Title: Efficacy of MVA-NP+M1 in the influenza H3N2 Human Challenge model | |||||||||||||
| Medical condition: influenza disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004386-24 | Sponsor Protocol Number: PEGACRO | Start Date*: 2015-12-04 | |||||||||||
| Sponsor Name:DIPARTIMENTO DI MEDICINA CLINICA E CHIRURGIA - UNIVERSITÀ DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
| Full Title: Effect of GH receptor antagonist on insulin resistance associated with acromegaly | |||||||||||||
| Medical condition: acromegaly | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-000098-35 | Sponsor Protocol Number: ANEPRO_2016_78 | Start Date*: 2017-07-31 |
| Sponsor Name:SERVICIO DE ANESTESIOLOGÍA Y REANIMACIÓN HOSPITAL UNIVERSITARIO LA PAZ | ||
| Full Title: COMPARATIVE STUDY OF NAUTICS AND VOMITING IN THREE ANESTHETICAL REGIMENS: INTRAVENOUS, INHALATORY AND MIXED. | ||
| Medical condition: Arthroscopy for Temporomandibular | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002742-42 | Sponsor Protocol Number: 2013DM19 | Start Date*: 2014-12-23 |
| Sponsor Name:University of Dundee/ NHS Tayside | ||
| Full Title: Research into the Effect Of SGLT2 inhibition on left ventricular Remodelling in patients with heart failure and diabetes Mellitus | ||
| Medical condition: Type 2 diabetes and Heart Failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-003966-42 | Sponsor Protocol Number: 71691 | Start Date*: 2021-02-16 |
| Sponsor Name:Erasmus MC | ||
| Full Title: Adjuvant hepatic arterial infusion pump chemotherapy after repeat hepatectomy for patients with recurrent colorectal liver metastases without a history of extrahepatic disease – a phase II study | ||
| Medical condition: LIver recurrence after hepatectomy for CRLM. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000866-41 | Sponsor Protocol Number: 2019001_mife50 | Start Date*: 2021-02-02 |
| Sponsor Name:Women on Web International Foundation | ||
| Full Title: Combined Phase II/ III Multicentre Single-arm Trial of a Mifepristone 50 mg as a weekly Contraceptive | ||
| Medical condition: Prevention of unwanted pregnancy | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004863-29 | Sponsor Protocol Number: 1M | Start Date*: 2013-02-18 |
| Sponsor Name:University Hospitals Leuven (Gasthuisberg) [...] | ||
| Full Title: Direct thrombin inhibitors versus low molecular weight heparins as thromboprophylaxis in Staphylococcus aureus bacteraemia. A prospective randomized controlled academic single-centre feasibility st... | ||
| Medical condition: staphylococcus aureus bacteraemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-005196-17 | Sponsor Protocol Number: BCX1812-211 | Start Date*: 2007-01-22 | |||||||||||
| Sponsor Name:BioCryst Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A phase II, Multicenter, Randomised, Double-Mask, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Intramuscular Peramivir in Subjects with Uncomplicated Acute Influenza | |||||||||||||
| Medical condition: Uncomplicated Acute Influenza | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001938-42 | Sponsor Protocol Number: UCL-ONCO2011-01 | Start Date*: 2012-01-24 |
| Sponsor Name:Cliniques universitaires Saint-Luc | ||
| Full Title: Randomized Phase II Study of CABAZITAXEL versus METHOTREXATE in patients with recurrent or metastatic squamous cell carcinoma of the head and neck previously treated with platinum-based therapy | ||
| Medical condition: To evaluate the efficacy of cabazitaxel in patients with palliative head and neck previously treated with platinum-based therapy. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-023461-22 | Sponsor Protocol Number: ET2010-077 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:CENTRE LEON BERARD | |||||||||||||
| Full Title: Efficacité et tolérance d’emplâtres de lidocaïne à 5% (Versatis® 5%) dans les douleurs neuropathiques et dans les douleurs de crises vaso-occlusives drépanocytaires de l’enfant, de l’adolescent et ... | |||||||||||||
| Medical condition: Enfants, adolescents ou jeunes adultes présentant soit des douleurs neuropathiques pures ou mixtes soit des douleurs de crises vaso-occlusives drépanocytaires, localisées, superficielles | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013878-40 | Sponsor Protocol Number: 09.08 | Start Date*: 2009-08-24 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Phase II trial of Cetuximab in combination with chemotherapy (Carboplatinum and Navelbine) for patients with platinum-resistant head- and neckcancer | |||||||||||||
| Medical condition: Platinum-resistant head and neck cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-004232-22 | Sponsor Protocol Number: SIC | Start Date*: 2009-03-24 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Phase II study with cetuximab, irinotecan and sunitinib (CIS) for patients with treatment resistant colorectal cancer | |||||||||||||
| Medical condition: Patients resistant to treatment of colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001430-25 | Sponsor Protocol Number: FPS-CES-2017-01 | Start Date*: 2017-11-07 |
| Sponsor Name:Fundación Pública Andaluza Progreso y Salud | ||
| Full Title: The effects of sufentanil or morphine added to hyperbaric bupivacaine in spinal anaesthesia for elective caesarean section. | ||
| Medical condition: CESAREAN | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
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