- Trials with a EudraCT protocol (99)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (5,530)
99 result(s) found for: TRA.
Displaying page 1 of 5.
EudraCT Number: 2007-007931-25 | Sponsor Protocol Number: 158/06 | Start Date*: 2006-11-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Prospective evaluation on the role exerted by the association of ethinylestradiol (0,03 mg) plus clormadinone acetate (2 mg) or ethinylestradiol (0,02 mg) plus desogestrel (0,15 mg) on insulin sens... | |||||||||||||
Medical condition: Volontari sani | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005829-11 | Sponsor Protocol Number: 080908 | Start Date*: 2010-11-18 |
Sponsor Name:FUNDACION CV INVESTIGACION HOSPITAL DR PESET | ||
Full Title: Mifepristona en la prevención del síndrome de hiperestimulación ovárica en tratamientos de reproducción asistida | ||
Medical condition: Mifepristona en la prevención del síndrome de hiperestimulación ovárica en tratamientos de reproducción asistida | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005403-33 | Sponsor Protocol Number: LANEX | Start Date*: 2012-01-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA CARDARELLI | |||||||||||||
Full Title: Studio controllato, randomizzato, di fase II di trattamento neoadiuvante con Sorafenib prima dell'ablazione termica dell'epatocarcinoma di diamentro superiore ai 4 cm | |||||||||||||
Medical condition: liver cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003035-78 | Sponsor Protocol Number: 72/2006/U/Sper | Start Date*: 2006-07-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: SICUREZZA ED EFFICACIA DI CICLOSPORINA A BASSE DOSI IN ASSOCIAZIONE AD EVEROLIMUS NEL PROTEGGERE LA FUNZIONE RENALE NEI PAZIENTI CON TRAPIANTO DI CUORE | |||||||||||||
Medical condition: Heart transplant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005711-26 | Sponsor Protocol Number: IDI-DER-1-20070930 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:ISTITUTO DERMOPATICO IMMACOLATA | |||||||||||||
Full Title: An open prospective, monocenter, consecutive non randomized clinical trial on therapy with monoclonal antibodies anti-CD20 in the treatment of pemphigus vulgare or foliaceus, serious and resistant ... | |||||||||||||
Medical condition: Pemphigus vulgaris, pemphigus foliaceus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012049-46 | Sponsor Protocol Number: IEO S480/209 | Start Date*: 2010-07-29 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: Phase III, randomized, double blind trial on Vitamin D supplementation for resected stage II melanoma patients. | |||||||||||||
Medical condition: melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002668-42 | Sponsor Protocol Number: TRA-IV-17-1 | Start Date*: 2017-10-11 |
Sponsor Name:Laboratoires SMB S.A. | ||
Full Title: A randomised, interventional, double blind, crossover, controlled study to assess the effect of the administration of paracetamol on tramadol adverse events. | ||
Medical condition: healthy volunteers (symptomatic treatment of pain) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005354-68 | Sponsor Protocol Number: procalcitonina | Start Date*: 2006-09-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Confronto tra un regime terapeutico basato sui livelli sierici di procalcitonina rispetto ad un regime terapeutico standard in pazienti ospedalizzati per riacutizzazione di broncopneumopatia cronic... | |||||||||||||
Medical condition: Riacutizzazione infettiva BPCO. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003996-35 | Sponsor Protocol Number: IPERBRO | Start Date*: 2005-02-01 | |||||||||||
Sponsor Name:UNIVERSITA DEGLI STUDI DI UDINE | |||||||||||||
Full Title: randomized,double blind, placebo-controlled trial of the effect of treatment with 3 hypertonic salin solution on bronchiolitis | |||||||||||||
Medical condition: Nebulized 3 hypertonic saline solution to improve clinical outcomes in children with bronchiolitis | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000637-13 | Sponsor Protocol Number: CRAP-ACStrial | Start Date*: 2022-02-08 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA USL TOSCANA CENTRO | ||||||||||||||||||||||||||||
Full Title: Cardiac and renal protective effect of colchicine early on-admission administered in patient with acute coronaric syndrome in treatment with atorvastatin | ||||||||||||||||||||||||||||
Medical condition: sindrome coronarica acuta (ACS) statin-naive con indicazione ad una strategia invasiva di rivascolarizzazione che vengono ricoverati in reparto cardiologico. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002942-12 | Sponsor Protocol Number: P04737 | Start Date*: 2007-10-22 | |||||||||||
Sponsor Name:Schering-Plough Research Institute | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of SCH 530348 in Addition to Standard of Care in Subjects With a History of Atherosclerotic Dis... | |||||||||||||
Medical condition: Documented coronary artery disease, postischemic cerebrovascular disease or peripheral artery disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DK (Completed) NL (Completed) SE (Completed) PT (Completed) FI (Completed) CZ (Completed) GB (Completed) BE (Completed) IT (Completed) ES (Completed) AT (Completed) DE (Completed) PL (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002959-18 | Sponsor Protocol Number: PRN1008-017/ACT17125 | Start Date*: 2023-03-23 | |||||||||||
Sponsor Name:Principia Biopharma Inc | |||||||||||||
Full Title: An open label, two-arm, Phase 2a study to evaluate the effect of rilzabrutinib (PRN1008/SAR444671) on safety and disease activity in patients with IgG4-related disease | |||||||||||||
Medical condition: IgG4-related disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002809-31 | Sponsor Protocol Number: P04736 | Start Date*: 2008-04-30 | |||||||||||
Sponsor Name:Schering Plough Research Institute, a Division of Schering Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of SCH 530348 in Addition to Standard of Care in Subjects With Acute Coronary Syndrome: Thrombi... | |||||||||||||
Medical condition: Acute Coronary Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) FR (Completed) DK (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) PT (Prematurely Ended) DE (Prematurely Ended) NL (Completed) AT (Completed) ES (Prematurely Ended) IT (Prematurely Ended) HU (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016176-78 | Sponsor Protocol Number: 2009-016176-78 | Start Date*: 2010-02-08 | |||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||||||||||||
Full Title: Terapy with everolimus in liver transplant. | |||||||||||||||||||||||
Medical condition: liver transplant | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014376-22 | Sponsor Protocol Number: MC/PR/1404/003/09 | Start Date*: 2010-02-15 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: MULTICENTRE, RANDOMIZED, DOUBLE-BLIND, PLACEBOCONTROLLED, TWO-ARM PARALLEL GROUPS STUDY DESIGN TO DEMONSTRATE THE EFFICACY AND TOLERABILITY OF A SINGLE DOSE OF BDP SUSPENSION FOR NEBULISATION 16... | |||||||||||||
Medical condition: CROUP (acute laryngotracheobronchitis) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005891-28 | Sponsor Protocol Number: CORICA | Start Date*: 2008-10-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Perspective evaluation on the role practiced by three different contraceptive hormonal on l I risk cardiovascular in young women: impact on the sensibility' insulinica | |||||||||||||
Medical condition: GIOVANI DONNE TRA 18 E 35 ANNI | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000515-14 | Sponsor Protocol Number: GPIAP | Start Date*: 2008-01-21 |
Sponsor Name:AZIENDA SANITARIA LOCALE 9 DI GROSSETO | ||
Full Title: Utility og GPIIb/IIIa inhibitor in patients with medium-low clinical risk but with high risk of periprocedural necrosis in coronary lesion. | ||
Medical condition: Patients with medium-low clinical risk but with high risk of periprocedural necrosis in coronary lesion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000964-16 | Sponsor Protocol Number: 1311-BCN-138-DG | Start Date*: 2015-03-30 |
Sponsor Name:IVI Valencia | ||
Full Title: Uterine fibroids: Impact of ulipristal acetate 10 mg on ART results. | ||
Medical condition: Uterine Fibroids and Assisted Reproduction | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-013662-33 | Sponsor Protocol Number: GICNO 08.001 | Start Date*: 2009-12-04 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: PROSPECTIVE EVALUATION OF SERUM MALDI TOF MS PROTEOMIC PROFILE PREDICTIVE OF OUTCOME IN PATIENTS WITH GLIOBLASTOMA MULTIFORME TREATED WITH STANDARD TREATMENT STRATIFIED ACCORDING TO MGMT | |||||||||||||
Medical condition: patients affected by GBM | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004606-18 | Sponsor Protocol Number: WASH-OUT | Start Date*: 2018-06-19 | |||||||||||
Sponsor Name:UNIVERSITÀ CAMPUS BIO-MEDICO DI ROMA | |||||||||||||
Full Title: Terapia di disassuefazione con metilprednisolone e diazepam ev in pazienti affetti da cefalea cronica con uso eccessivo di sintomatici | |||||||||||||
Medical condition: Emicrania Cronica e Cefalea da Iperuso di Farmaci | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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