- ICH GCP
- EU Clinical Trials Registry
Latest Trials
EudraCT Number: 2004-003809-25 | Sponsor Protocol Number: L-9134 | Start Date: 2004-12-20 | ||||||
Sponsor Name: Sanofi-Synthelabo Co. Ltd. | ||||||||
Full Title: Comparison of the efficacy and tolerability of drotaverine 80 mg or ibuprofen 400 mg administered alone with their combination for the treatment of primary and secondary dysmenorrhea | ||||||||
Medical condition: A NO-SPA és az ibuprofen kombinációja elfogadott és Magyarországon gyakran használták a nőgyógyászati gyakorlatban sok évvel ezelőtt. A kombináció használatával kapcsolatos súlyos mellékhatásról ne... | ||||||||
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Population Age: Adults | Gender: Female | |||||||
Trial protocol: HU (Prematurely Ended) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002013-36 | Sponsor Protocol Number: ACA-SPAI-03-03 | Start Date: 2004-12-17 | ||||||
Sponsor Name: CONCEPCION MORO SERRANO | ||||||||
Full Title: A PROSPECTIVE DOUBLE BLIND AND RANDOMIZED STUDY ON THE EFFECT OF TRANDOLAPRIL, IN MAINTAINING SINUS RHYTHM IN PATIENTS WITH LONG-LASTING PERSISTENT ATRIAL FIBRILLATION. ESTUDIO PROSPECTIVO, DOBLE ... | ||||||||
Medical condition: PACIENTES CON FA PERSISTENTE DE LARGA DURACÍON. | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: ES (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001943-31 | Sponsor Protocol Number: SEC-2004-001 | Start Date: 2004-12-17 | |||||||||||
Sponsor Name: Sociedad Española de Cardiología | |||||||||||||
Full Title: ESTUDIO ALEATORIZADO PARA COMPARAR LA EFICACIA Y SEGURIDAD DE LA FIBRINOLISIS O LA ANGIOPLASTIA PRIMARIA COMO TRATAMIENTO INICIAL DE REPERFUSIÓN EN LOS PACIENTES DE EDAD AVANZADA (>/=75 AÑOS) CON I... | |||||||||||||
Medical condition: Acute Myocardial infarction | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001190-25 | Sponsor Protocol Number: A6291015 | Start Date: 2004-12-17 | ||||||
Sponsor Name: Pfizer Ltd | ||||||||
Full Title: A Double-blind, Proof of Concept Trial of the Use of Pegvisomant to Reduce Urinary Albumin Excretion in Type 1 and Type 2 Diabetic Patients Treated with Angiotensin Convertase Inhibitors/Angiotensi... | ||||||||
Medical condition: Diabetic nephropathy DN (Diabetes mellitus (DM) type I and type II with renal manifestations). MedDRA classification code : 10061835, 10045236 and 10045250 (Version 7.0, Level LLT) | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: LT (Completed) CZ (Completed) DE (Completed) GB (Completed) ES (Completed) DK (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-000616-70 | Sponsor Protocol Number: HMR1964D/3001 | Start Date: 2004-12-17 | ||||||
Sponsor Name: Aventis Pharmaceuticals, Inc. | ||||||||
Full Title: Efficacy and safety of insulin glulisine compared with insulin lispro in children and adolescents with type 1 diabetes mellitus: a 26-week, multicenter, open, parallel clinical trial | ||||||||
Medical condition: Type 1 diabetes mellitus | ||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||
Trial protocol: DK (Completed) NO (Completed) FI (Completed) SE (Completed) HU (Completed) GB (Completed) DE (Completed) BE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002889-38 | Sponsor Protocol Number: OV-WV03 | Start Date: 2004-12-16 | ||||||
Sponsor Name: OmniVision GmbH | ||||||||
Full Title: Randomisierte, kontrollierte, doppelblinde klinische Prüfung zur Untersuchung der Wirksamkeit und Verträglichkeit von Novesine® 0,4% Augentropfen im Vergleich zur Augentropfengrundlage bei zur Tono... | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-002757-31 | Sponsor Protocol Number: CLAF237A 2303E1 | Start Date: 2004-12-16 | ||||||
Sponsor Name: Novartis Sverige AB | ||||||||
Full Title: A 28-Week Extension to a Multicenter, Double-Blind, Randomized, Parallel-Group Study to Compare the Effect of 24 Weeks Treatment with LAF237 (50 mg qd or bid) to Placebo as Add-On Therapy in Patien... | ||||||||
Medical condition: Type 2 Dibetes | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-003962-14 | Sponsor Protocol Number: BLO K022 | Start Date: 2004-12-16 | ||||||
Sponsor Name: Takeda Pharma GmbH | ||||||||
Full Title: Candesartan "added" Treatment for Optimisation of Heart Failure (HF) Therapy - Effects on BNP and other HF associated Parameters. An open, non-controlled and multicentre trial | ||||||||
Medical condition: Heart failure | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-000492-18 | Sponsor Protocol Number: 1050/04 | Start Date: 2004-12-16 | |||||||||||
Sponsor Name: POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Insulin resistance and endothelial dysfunction TNF-Alpha dependent in patients with rheumatoid arthritis or metabolic syndrome | |||||||||||||
Medical condition: Metabolic Syndrome and Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002940-82 | Sponsor Protocol Number: CLAF237A2355 | Start Date: 2004-12-16 | ||||||
Sponsor Name: Novartis Pharma Services AG | ||||||||
Full Title: A multicenter, randomized, double-blind, active controlled study to compare the effect of 24 weeks treatment with combination therapy of LAF237 and pioglitazone to LAF237 monotherapy or pioglitazon... | ||||||||
Medical condition: Type II Diabetes | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SK (Completed) CZ (Completed) GB (Completed) IT (Completed) | ||||||||
Trial results: View results |