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EudraCT Number: 2006-001896-39 | Sponsor Protocol Number: DUO 05 | Start Date: 2006-12-07 | |||||||||||
Sponsor Name: SOFAR SPA | |||||||||||||
Full Title: Evaluation of symbiotic effect on the intestinal function in idiopathic chronic constipation. Multicenter, randomised, cross-over, double-blind, placebo-controlled study | |||||||||||||
Medical condition: CIdiopathic chronic constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001623-18 | Sponsor Protocol Number: EGF102988 | Start Date: 2006-12-07 | |||||||||||
Sponsor Name: GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Multi-centre, Phase III Study of Post-Operative Adjuvant Lapatinib or Placebo and Concurrent Chemoradiotherapy Followed by Maintenance Lapatinib or P... | |||||||||||||
Medical condition: Resected Squamous Cell Carcinoma of the Head and Neck | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IE (Completed) GR (Completed) AT (Completed) SK (Completed) GB (Completed) DE (Completed) CZ (Completed) PT (Prematurely Ended) EE (Completed) HU (Completed) IT (Completed) LV (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005654-53 | Sponsor Protocol Number: BroSin 05 | Start Date: 2006-12-07 | ||||||
Sponsor Name: Ursapharm Arzneimittel GmbH & Co. KG | ||||||||
Full Title: "Explorative triple-arm dosis-finding study for examination about the effectivity and tolerance of Bromelain by acute sinusitis" | ||||||||
Medical condition: Therapy of acute sinusitis | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-002438-37 | Sponsor Protocol Number: 2005/VCC/0018(WCTU02) | Start Date: 2006-12-07 | |||||||||||
Sponsor Name: Velindre NHS Trust | |||||||||||||
Full Title: A randomised phase III clinical trial investigating the effect of FRAGMin® Added to standard Therapy In patients with lung Cancer | |||||||||||||
Medical condition: Lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005626-24 | Sponsor Protocol Number: 1247 | Start Date: 2006-12-07 | |||||||||||
Sponsor Name: POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: PHASE II STUDY ON PEMETREXED IN ADVANCED AND/OR RECURRENT CERVICAL CANCER | |||||||||||||
Medical condition: advanced or metastatic cervical cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004398-89 | Sponsor Protocol Number: 380104 | Start Date: 2006-12-06 | |||||||||||
Sponsor Name: Medinova AG | |||||||||||||
Full Title: Comparative Study of the Efficacy of 10 mg Dequalinium Chloride (Fluomizin®) in the Local Treatment of Bacterial Vaginosis | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001846-15 | Sponsor Protocol Number: CSUC-01/06 | Start Date: 2006-12-06 | ||||||
Sponsor Name: InDex Pharmaceuticals AB | ||||||||
Full Title: A placebo-controlled, randomised, double-blind, single dose proof of concept study of Kappaproct, in steroid resistant or steroid dependent patients with ulcerative colitis of mild to moderate degree | ||||||||
Medical condition: Active ulcerative colitis in steroid refractory or steroid dependent patients | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Prematurely Ended) | ||||||||
Trial results: (No results available) |
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. | ||||||||
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Population Age: Adults | Gender: Male | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005082-19 | Sponsor Protocol Number: RB23EZ | Start Date: 2006-12-06 | |||||||||||
Sponsor Name: Research Innovation Services, University of Nottingham | |||||||||||||
Full Title: Effect of an angiotensin receptor antagonist on cerebral blood flow, cerebral perfusion pressure, and systemic and peripheral haemodynamics in patients with recent stroke. | |||||||||||||
Medical condition: Patients who have hypertension in the context of recent stroke. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000474-42 | Sponsor Protocol Number: CL2-90652-002 | Start Date: 2006-12-06 | |||||||||||
Sponsor Name: INSTITUT DE RECHERCHES INTERNATIONALES SERVIER | |||||||||||||
Full Title: Safety and effects on blood pressure of a daily dose of 0.025 to 0.135 milligram per kilogram of S 90652, a paediatric formulation of perindopril, in hypertensive children having received S 90652 -... | |||||||||||||
Medical condition: Arterial Hypertension | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |