Ultime prove


EudraCT Number: 2006-003302-25 Sponsor Protocol Number: PRG-OXYCODONE-06/01 Start Date: 2006-11-30
Sponsor Name: Barts and The London NHS Trust
Full Title: A prospective, randomised, double-blind, placebo-controlled trial to assess the respiratory effects of oxycodone versus morphine in anaesthetised patients
Medical condition: Patients scheduled to undergo surgery of more than 30 minutes duration under general anaesthesia will be recruited. We are not investigating a medical disease.
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: View results

EudraCT Number: 2006-001062-17 Sponsor Protocol Number: ASF-1096-201/250912BS Start Date: 2006-11-30
Sponsor Name: Astion Danmark A/S
Full Title: Efficacy and safety of ASF-1096 cream 0.5% in the treatment of patients with newly developed discoid lupus erythymatosus (DLE) lesions. A multi centre clinical phase 2, placebo controlled and doubl...
Medical condition: Male or female patients with a clinical diagnosis of either Discoid Lupus Erythmatosus or Systemic Lupus Erythmatosus and at least one newly developed, sharply demarcated DLE lesion.
Disease: Version SOC Term Classification Code Term Level
8.1 10025138 Lupus erythematosus discoides LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: GB (Completed) SE (Prematurely Ended)
Trial results: (No results available)
EudraCT Number: 2006-001254-27 Sponsor Protocol Number: P051205 Start Date: 2006-11-30
Sponsor Name: ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
Full Title: Open randomised prospective comparative multi-centre intervention study of patients with cystic fibrosis and early diagnosed diabetes mellitus
Medical condition: Patients atteints de mucoviscidose, chez lesquels un diagnostic de diabète a été fait par hyperglycémie provoquée orale (HGPO)
Disease: Version SOC Term Classification Code Term Level
8.1 10012594 DIABETES PT
Population Age: Adolescents, Under 18, Adults, Elderly Gender: Male, Female
Trial protocol: FR (Ongoing)
Trial results: (No results available)

EudraCT Number: 2004-001672-39 Sponsor Protocol Number: CARDIOCC2004 Start Date: 2006-11-30
Sponsor Name: Dr Moya Mur
Full Title: EFECTO PROTECTOR DE LA ATORVASTATINA SOBRE LA FUNCION MICROVASCULAR CORONARIA Y FUNCION COGNITIVA CEREBRAL EN PACIENTES SOMETIDOS A REVASCULARIZACION CORONARIA
Medical condition: CARDIOPATIA ISQUEMICA
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: ES (Ongoing)
Trial results: (No results available)
EudraCT Number: 2006-002165-39 Sponsor Protocol Number: P04887 Start Date: 2006-11-30
Sponsor Name: Schering Plough Research Institute, a division of Schering Corporation
Full Title: Study of the Efficacy and Safety of SCH486757 in Subjects With Chronic Idiopathic Cough
Medical condition: Chronic Idiopathic Cough
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: View results

EudraCT Number: 2006-002324-41 Sponsor Protocol Number: PH2/051 Start Date: 2006-11-30
Sponsor Name: Cancer Research UK
Full Title: A Cancer Research UK Randomised Multicentre Phase II Trial of the DNA-hypomethylating Agent, 5-Aza-2'-deoxycytidine(Decitabine) given intravenously in Combination with Carboplatin, versus Carboplat...
Medical condition: Progressive, advanced ovarian cancer
Disease: Version SOC Term Classification Code Term Level
8.1 10033128 Ovarian cancer LLT
Population Age: Adults, Elderly Gender: Female
Trial protocol: GB (Prematurely Ended)
Trial results: View results
EudraCT Number: 2006-003142-42 Sponsor Protocol Number: SC12267-3-2005 Start Date: 2006-11-30
Sponsor Name: 4SC AG
Full Title: A Randomized, Double Blind, Placebo-controlled, Proof of Concept Study to evaluate Efficacy, Safety and Pharmacokinetics of two Different Doses of SC12267 (20mg, 35 mg) in Patients with Rheumatoid ...
Medical condition: Active Rheumatoid Arthritis
Disease: Version SOC Term Classification Code Term Level
8.1 10039073 Rheumatoid arthritis PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: View results

EudraCT Number: 2006-002757-72 Sponsor Protocol Number: NEOSH101-CLIN-AGA003 Start Date: 2006-11-30
Sponsor Name: Neosil Inc.
Full Title: A Phase 2 Multicenter, Randomized, Placebo- and Comparator Controlled, Double-Blind Parallel Group Study to Evaluate the Safety and Efficacy of Topical NEOSH101 in the Treatment of Androgenetic Alo...
Medical condition: The study will be performed in male subjects with androgenetic alopecia, Norwood -Hamilton grades III - IV.
Disease: Version SOC Term Classification Code Term Level
8.1 10001760 Alopecia LLT
Population Age: Adults Gender: Male
Trial protocol: DE (Completed)
Trial results: (No results available)
EudraCT Number: 2006-004977-91 Sponsor Protocol Number: ANA06104 Start Date: 2006-11-30
Sponsor Name: Universitätsklinikum Mannheim, Klinik für Anästhesiologie
Full Title: Inhalative Sedierung mit Sevofluran im Vergleich zu Propofol bei beatmeten, postoperativen Intensivpatienten – Einfluss auf Extubationszeiten und Aufwachverhalten, Nieren- und Leberfunktion, Hämody...
Medical condition: Der Einsatz von Sevofluran im Vergleich zur konventionellen Sedierung mit Propofol soll in Bezug auf Sedierungsgrad unter Beatmung, Extubationszeit und Aufwachverhalten, Hämodynamik, Kardioprotekti...
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: (No results available)

EudraCT Number: 2006-005096-17 Sponsor Protocol Number: 0633-009 Start Date: 2006-11-30
Sponsor Name: Merck & Co., Inc
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study, Conducted Under In-House blinding Conditions of MK-0633 in Patients With COPD
Medical condition: Chronic Obstructive Pulmonary Disease (COPD)
Disease: Version SOC Term Classification Code Term Level
8.1 10010952 COPD LLT
Population Age: Adults, Elderly Gender: Male
Trial protocol: LT (Completed)
Trial results: View results
3
Sottoscrivi