- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Clathrate.
Displaying page 1 of 1.
| EudraCT Number: 2006-004899-13 | Sponsor Protocol Number: 310882 | Start Date*: 2008-01-16 |
| Sponsor Name:Bayer Schering Pharma AG | ||
| Full Title: A multi-center, open-label, randomized, controlled, parallel-group study to assess efficacy and safety of an extended flexible regimen of the combined oral contraceptive SH T00186D (0.02 mg ethinyl... | ||
| Medical condition: women suffering from primary dysmenorrhea | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DE (Completed) GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002125-32 | Sponsor Protocol Number: 308683 | Start Date*: 2005-12-22 |
| Sponsor Name:Bayer Schering Pharma AG | ||
| Full Title: A multicenter, open, randomized, parallel-group comparison to assess the safety and efficacy of the oral contraceptive SH T 00186 D (0.02 mg ethinylestradiol as betadex clathrate and 3 mg drospiren... | ||
| Medical condition: healthy volunteers requesting oral contraception | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-001789-13 | Sponsor Protocol Number: QUINA/2012 | Start Date*: 2012-11-16 |
| Sponsor Name:Instituto de Investigacion Sanitaria La e | ||
| Full Title: Double-blind, randomized, controlled contraceptives, parallel group, to assess the effect on nerve fibers in patients diagnosed with endometriosis grade III / IV symptomatic ascending-dose oral qui... | ||
| Medical condition: Endometriosis grade III/IV | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-004522-16 | Sponsor Protocol Number: DU176b-C-U301 | Start Date*: 2009-05-20 | |||||||||||
| Sponsor Name:Daiichi Sankyo Pharma Development | |||||||||||||
| Full Title: A PHASE 3, RANDOMIZED, DOUBLE-BLIND, DOUBLE-DUMMY, PARALLEL GROUP, MULTI-CENTER, MULTI-NATIONAL STUDY FOR EVALUATION OF EFFICACY AND SAFETY OF DU-176B VERSUS WARFARIN IN SUBJECTS WITH ATRIAL FIBRIL... | |||||||||||||
| Medical condition: Reduction of Stroke and/or systemic embolic event (SEE) in subjects with atrial fibrillation (AF). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) GB (Completed) SE (Completed) EE (Completed) FI (Completed) NL (Completed) PT (Completed) DK (Completed) ES (Completed) CZ (Completed) IT (Completed) BG (Completed) HU (Completed) SK (Completed) GR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019902-17 | Sponsor Protocol Number: BAY86-5300/14701 | Start Date*: 2010-12-09 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: A multicenter, open-label, randomized, controlled, two-arm study to assess compliance with daily tablet intake of women on treatment with the oral contraceptive SH T00186D/BAY 86-5300 (0.02 mg ethi... | |||||||||||||
| Medical condition: Contraception | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003148-21 | Sponsor Protocol Number: DU176b-F-E308 | Start Date*: 2014-06-17 | |||||||||||
| Sponsor Name:Daiichi Sankyo Development Ltd | |||||||||||||
| Full Title: A prospective, randomised, open-label, blinded endpoint evaluation (PROBE) parallel group study comparing edoxaban (DU-176b) with enoxaparin/warfarin followed by warfarin alone in subjects undergoi... | |||||||||||||
| Medical condition: Stroke and thromboembolism prevention in patients with non-valvular atrial fibrillation (NVAF) undergoing planned electrical cardioversion. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) BE (Completed) DE (Completed) GB (Completed) HU (Completed) IT (Completed) DK (Completed) ES (Completed) AT (Completed) CZ (Completed) NL (Completed) RO (Completed) BG (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014290-40 | Sponsor Protocol Number: DU176b-D-U305 | Start Date*: 2010-02-10 | ||||||||||||||||
| Sponsor Name:Daiichi Sankyo Development Limited | ||||||||||||||||||
| Full Title: A phase 3, randomized, double-blind, double-dummy, parallel-group, multi-center, multi-national study for the evaluation of efficacy and safety of (LMW) heparin/edoxaban versus (LMW) heparin/warfar... | ||||||||||||||||||
| Medical condition: Reduction of the risk of symptomatic recurrent venous thromboembolic complications in patients with acute symptomatic deep vein thrombosis (DVT) and/or pulmonary embolism (PE) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) HU (Completed) DE (Completed) SE (Completed) FR (Completed) EE (Completed) BE (Completed) AT (Completed) ES (Completed) DK (Completed) CZ (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2004-002181-38 | Sponsor Protocol Number: WARCEF | Start Date*: 2004-10-22 |
| Sponsor Name:NIH-National Institut of Health - NINDS-National Institut of Neurogical Disorders and Stroke | ||
| Full Title: Warfarin versus Aspirin in Reduced Ejection Fraction. | ||
| Medical condition: Patients with left ventricular disfunction with ejection fraction less or equal to 35%. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) SK (Completed) GB (Completed) | ||
| Trial results: (No results available) | ||
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