- Trials with a EudraCT protocol (69)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
69 result(s) found for: Non communicable diseases.
Displaying page 1 of 4.
EudraCT Number: 2004-004693-87 | Sponsor Protocol Number: 2004-04 | Start Date*: 2004-11-03 | |||||||||||
Sponsor Name:OSPEDALE SACRO CUORE-DON CALABRIA | |||||||||||||
Full Title: Randomized study on therapy of Strongyloides stercoralis invasion: ivermectine VS thiabendazole | |||||||||||||
Medical condition: Strongyloidiasis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004718-40 | Sponsor Protocol Number: MELCOM-1 | Start Date*: 2011-07-18 | |||||||||||
Sponsor Name:AISAR ASSOCIAZIONE ITALIANA PER LO STUDIO DEGLI ANTIMICROBICI E DELLE RESISTENZE | |||||||||||||
Full Title: Activities of Metronidazole + Clotrimazole in the treatment and prophylaxis of recurrent vaginal infections recurrent Candida albicans and Candida albicans spp do not. | |||||||||||||
Medical condition: women with vaginal infections by Candida albicans and non-albicans Candida spp relapsing recurrent (≥ 4 events / year) in the acute phase of the disease. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000609-43 | Sponsor Protocol Number: V71P4S | Start Date*: 2006-05-22 | |||||||||||
Sponsor Name:CHIRON | |||||||||||||
Full Title: A Phase II, Open Label, Uncontrolled, Multi Center Study to Evaluate Safety and Immunogenicity of AGRIPPAL S1 Surface Antigen, Inactivated, Influenza Vaccine, Formulation 2006-2007, when Administer... | |||||||||||||
Medical condition: Active influenza immunoprofilaxis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024644-15 | Sponsor Protocol Number: 2010-024644-15 | Start Date*: 2012-02-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA DELLA SECONDA UNIVERSITA' DEGLI STUDI DI NAPOLI | |||||||||||||
Full Title: Concomitant therapy with levofloxacyn versus sequential therapy with levofloxacin for eradication of H. pylori infection | |||||||||||||
Medical condition: Helicobacter pylori infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003281-25 | Sponsor Protocol Number: ALBIOS STUDY | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:OSPEDALE MAGGIORE DI MILANO (IRCCS) | |||||||||||||
Full Title: Efficacy of albumin administration for volume replacement in patients with severe sepsis or septic shock | |||||||||||||
Medical condition: Patients with severe sepsis or septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005078-10 | Sponsor Protocol Number: FARM7X9F8K | Start Date*: 2008-10-20 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA VINCENZO MONALDI DI NAPOLI | |||||||||||||
Full Title: RANDOMISED, OPEN-LABEL CLINICAL TRIAL ON THE EFFICACY OF COLISTIN PLUS RIFAMPICIN TREATMENT VERSUS COLISTIN ALONE FOR SEVERE INFECTIONS BY MULTIDRUG-RESISTANT ACINETOBACTER BAUMANNII | |||||||||||||
Medical condition: Severe nosocomial infections due to multi-drug resistant Acinetobacter baumannii | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006132-24 | Sponsor Protocol Number: CDEB025A2313 | Start Date*: 2012-05-18 | |||||||||||
Sponsor Name:Novartis Farmaceutica, S.A. | |||||||||||||
Full Title: A multi-centre 3-year follow-up study to assess the viral activity in patients who failed to achieve sustained virologic response in Novartis-sponsored alisporivir studies for chronic hepatitis C p... | |||||||||||||
Medical condition: Chronic hepatitis C patients who failed to achieve sustained virologic response (SVR24) on alisporivir or direct-acting antivirals (DAA) in previous Novartis-sponsored studies. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) HU (Prematurely Ended) GB (Completed) PL (Prematurely Ended) IT (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005884-29 | Sponsor Protocol Number: CRU-Unipg2020-12 | Start Date*: 2021-04-28 | |||||||||||
Sponsor Name:UNIVERSITà DEGLI STUDI DI PERUGIA | |||||||||||||
Full Title: EFFICACY AND SAFETY OF HEPARIN THROMBOPROPHYLAXIS IN PATIENTS WITH COVID-19 AND RESPIRATORY FAILURE: AN OPEN LABEL RANDOMIZED STUDY. The RESPECT-COVID (RESPiratory failure and hEparin Clinical Tria... | |||||||||||||
Medical condition: Patients with confirmed SARS-CoV-2 infection and respiratory failure will be randomized to receive two different doses of low molecular weight heparin (LMWH). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010598-19 | Sponsor Protocol Number: V71_10S | Start Date*: 2009-03-31 | |||||||||||
Sponsor Name:NOVARTIS VACCINES AND DIAGNOSTICS S.R.L. | |||||||||||||
Full Title: A Phase II, Open Label, Uncontrolled, Multi Center Study to Evaluate Safety and Immunogenicity of AGRIPPAL S1 Surface Antigen, Inactivated, Influenza Vaccine, Formulation 2009-2010, when Administer... | |||||||||||||
Medical condition: The virus strains responsible for influenza vary in an unpredictable fashion, therefore the type of virus as well as the magnitude of influenza activity changes from one winter to the other. Theref... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005624-10 | Sponsor Protocol Number: OVID-trial | Start Date*: 2021-05-06 | ||||||||||||||||
Sponsor Name:University Hospital Zurich | ||||||||||||||||||
Full Title: ENOXAPARIN FOR PRIMARY THROMBOPROPHYLAXIS IN AMBULATORY PATIENTS WITH CORONAVIRUS: THE MULTICENTER RANDOMIZED CONTROLLED OVID TRIAL | ||||||||||||||||||
Medical condition: Patients diagnosed with COVID-19, a novel viral disease characterized by severe systemic, pulmonary, and vessel inflammation and coagulation activation. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004035-88 | Sponsor Protocol Number: AntiCov | Start Date*: 2021-11-18 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: A randomized, open-label, active controlled, parallel group, multicenter phase 3 study to evaluate the efficacy and tolerability of Bamlanivimab and Etesevimab, Casirivimab and Imdevimab, and Sotro... | |||||||||||||
Medical condition: Patients with mild to moderate SARS-COV-2 infection. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003391-74 | Sponsor Protocol Number: 106794 | Start Date*: 2016-05-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: Persistence of hepatitis B antibodies, immunogenicity and safety of GSK Biologicals’ hepatitis B vaccine, Engerix™-B Kinder (SKF103860) challenge dose, in adolescents vaccinated with four doses of ... | |||||||||||||
Medical condition: Immunisation against infection caused by all known subtypes of hepatitis B virus. | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002821-41 | Sponsor Protocol Number: 106793 | Start Date*: 2014-01-21 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: Persistence of hepatitis B antibodies, immunogenicity and safety of GSK Biologicals’ hepatitis B vaccine EngerixTM-B Kinder (SKF103860) challenge dose in adolescents vaccinated with four doses of I... | |||||||||||||
Medical condition: Hepatitis B | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003470-47 | Sponsor Protocol Number: 74730.041.20 | Start Date*: 2020-08-27 | |||||||||||
Sponsor Name:UMCU Utrecht [...] | |||||||||||||
Full Title: BACILLUS CALMETTE-GUÉRIN VACCINATION TO PREVENT SERIOUS RESPIRATORY TRACT INFECTION AND COVID-19 IN VULNERABLE ELDERLY – AN ADAPTIVE RANDOMIZED CONTROLLED TRIAL | |||||||||||||
Medical condition: Protection Covid infection by patients with chronic diseases or major surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000173-22 | Sponsor Protocol Number: 2012-000173-22 | Start Date*: 2012-07-20 | ||||||||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||||||||||||||||||
Full Title: HEALTHCARE ASSOCIATED BACTERIAL INFECTIONS IN HOSPITALIZED CIRRHOTIC PATIENTS. RANDOMIZED TRIAL:EMPIRICAL TRADIDIONAL ANTIBIOTIC THERAPY VS SECOND LINE THERAPY | ||||||||||||||||||
Medical condition: Healthcare-associeted bacterial infections in hospitalized cirrhotic patients. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002460-27 | Sponsor Protocol Number: 1.1 | Start Date*: 2013-02-04 | ||||||||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | ||||||||||||||||||
Full Title: Preoperative skin preparation to lower surgical site infection in breast cancer surgery: Povidone – iodine 10% aqueous solution versus 2%chlorhexidine in 70% isopropyl alcohol (ChloraPrep, Cardina... | ||||||||||||||||||
Medical condition: PATIENTS SCHEDULED FOR SURGERY | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022762-27 | Sponsor Protocol Number: PEN1011 | Start Date*: 2010-11-09 | |||||||||||
Sponsor Name:Klinisk Farmakologisk Afdeling, Bispebjerg | |||||||||||||
Full Title: Studiets formål er, at undersøge hvorvidt v-penicillin og trimethoprim inducerer oxidativt stress i raske frivillige forsøgsdeltagere. En eventuel induktion vurderes ud fra målinger på 8-oxoGuo- og... | |||||||||||||
Medical condition: Oxidative stress induced by antibiotics | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019194-15 | Sponsor Protocol Number: CRCFC-ABLC003 | Start Date*: 2010-05-12 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ISTITUTI OSPITALIERI DI VERONA | ||||||||||||||||||
Full Title: Esplorative study to evaluate the tolerability of Amphotericin B lipid complex (Abelcet) by aerosol in patients with Cystic Fibrosis and Allergic Bronchopulmonary Aspergillosis (ABPA) | ||||||||||||||||||
Medical condition: Cystic Fibrosis and Allergic Bronchopulmonary Aspergillosis (ABPA) | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001433-74 | Sponsor Protocol Number: LOCAL/2017/CR-01 | Start Date*: 2017-06-29 | |||||||||||
Sponsor Name:CHU de NIMES | |||||||||||||
Full Title: Screening Anti-Fungal Exposure in Intensive Care Units – The French Cohort | |||||||||||||
Medical condition: The study will recruit patients in intensive care unit prescribed to receive any of the chosen systemic antifungal agents | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002484-60 | Sponsor Protocol Number: 2020-002484-6060 | Start Date*: 2021-07-12 | |||||||||||||||||||||
Sponsor Name:Odense Universityhospital | |||||||||||||||||||||||
Full Title: Intrapleural Fibrinolysis and DNase versus VATS for the treatment of pleural empyema: a randomized, controlled trial. | |||||||||||||||||||||||
Medical condition: Pleural Empyema | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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