- Trials with a EudraCT protocol (6,491)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
6,491 result(s) found for: Standard of care.
Displaying page 1 of 325.
EudraCT Number: 2015-002685-23 | Sponsor Protocol Number: ICT-107-301 | Start Date*: 2016-08-19 | |||||||||||
Sponsor Name:ImmunoCellular Therapeutics, Ltd. | |||||||||||||
Full Title: A Phase III randomized double-blind, controlled study of ICT-107 with maintenance temozolomide (TMZ) in newly diagnosed glioblastoma following resection and concomitant TMZ chemoradiotherapy. | |||||||||||||
Medical condition: Treatment of newly diagnosed glioblastoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) DE (Prematurely Ended) NL (Ongoing) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010190-20 | Sponsor Protocol Number: 0908010 | Start Date*: 2009-04-22 | |||||||||||
Sponsor Name:CHU Saint-Etienne | |||||||||||||
Full Title: DETECTION OF ACUTE RENAL FAILURE IN CRITICALLY ILL PATIENTS: A prospective evaluation of cystatin C diagnostic performance | |||||||||||||
Medical condition: critically ill patients hospitalised in inetnsive care unit | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001270-29 | Sponsor Protocol Number: EFC16858 | Start Date*: 2020-04-08 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: An adaptive Phase 2/3, randomized, open-label study assessing efficacy and safety of hydroxychloroquine for hospitalized patients with moderate to severe COVID-19 | |||||||||||||
Medical condition: Coronavirus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001904-41 | Sponsor Protocol Number: GETAFIX-2020 | Start Date*: 2020-05-20 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | |||||||||||||
Full Title: Glasgow Early Treatment Arm FavIpiravir : A randomized controlled study of favipiravir as an early treatment arm in COVID-19 patients | |||||||||||||
Medical condition: COVID-19 | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002853-21 | Sponsor Protocol Number: RGHT000405 | Start Date*: 2007-09-03 |
Sponsor Name:Belfast Health & Social Care Trust [...] | ||
Full Title: A randomized controlled trial of tea tree oil (5%) body wash versus standard body wash to prevent colonization with methicillin-resistant Staphylococcus aureus (MRSA) in critically ill adults | ||
Medical condition: Colonization with methicillin-resistant Staphylococcus aureus (MRSA) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-001227-41 | Sponsor Protocol Number: CSIC-FDA135-2021-01 | Start Date*: 2021-12-23 | |||||||||||
Sponsor Name:AGENCIA ESTATAL CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS, M.P. (CSIC) | |||||||||||||
Full Title: A Randomized, Open-label, Standard-of-care comparative, Repositioning Clinical Trial to Evaluate the Efficacy and Safety of FDA-135 in combination with standard of care in the Treatment of Infectio... | |||||||||||||
Medical condition: SARS-CoV-2 virus infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004705-59 | Sponsor Protocol Number: 406201215432 | Start Date*: 2013-12-17 |
Sponsor Name:Hôpital Erasme, ULB | ||
Full Title: Monocentric phase III clinical trial using citalopram (antidepressive compound fequently used in clinic) added to the standard of care (radio- combined with temozolomide chemotherapy and followed b... | ||
Medical condition: Newly diagnosed glioblastoma (primary highly malignant brain cancer) patients Under treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001228-17 | Sponsor Protocol Number: CSIC-FDA277-2021-01 | Start Date*: 2022-02-11 | |||||||||||
Sponsor Name:AGENCIA ESTATAL CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS, M.P. (CSIC) | |||||||||||||
Full Title: A Randomized, double-blind, Repositioning Clinical Trial, placebo controlled, to Evaluate the Efficacy and Safety of FDA-277 in combination with standard of care in the Treatment of Infection Cause... | |||||||||||||
Medical condition: SARS-CoV-2 virus infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003670-31 | Sponsor Protocol Number: BC-10433 | Start Date*: 2021-09-22 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Impact of Model-Informed Precision Dosing of Vancomycin in Adults: A randomized, controlled clinical trial | ||
Medical condition: Gram positive infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003614-40 | Sponsor Protocol Number: SVB800_001 | Start Date*: 2019-06-06 | |||||||||||
Sponsor Name:Bracco Imaging Spa | |||||||||||||
Full Title: MOLECULAR FLUORESCENCE-GUIDED SURGERY USING BEVA800 FOR THE ASSESSMENT OF TUMOR MARGINS DURING BREAST CONSERVING SURGERY OF PATIENTS WITH PRIMARY BREAST CANCER (MARGIN-II) | |||||||||||||
Medical condition: Primary breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002708-25 | Sponsor Protocol Number: RIVAROXACS3001 (BAY59-7939/13194) | Start Date*: 2008-11-27 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Event-Driven Multicenter Study to Evaluate the Efficacy and Safety of Rivaroxaban in Subjects with a Recent Acute Coronary Syndrome The ATLAS ACS 2 ... | |||||||||||||
Medical condition: Acute Coronary Syndrome (ACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) LT (Completed) DE (Completed) PT (Completed) SK (Completed) HU (Completed) FR (Completed) DK (Completed) GB (Completed) NL (Completed) ES (Completed) IT (Completed) LV (Completed) CZ (Completed) BG (Completed) BE (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000037-14 | Sponsor Protocol Number: NEOD001-301 | Start Date*: 2021-09-01 | |||||||||||
Sponsor Name:Prothena Biosciences Limited | |||||||||||||
Full Title: A Phase 3, Randomized, Multicenter, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Birtamimab Plus Standard of Care vs. Placebo Plus Standard of Care in Mayo Stage IV Subjects with ... | |||||||||||||
Medical condition: AL amyloidosis involves a hematologic disorder caused by clonal plasma cells that produce misfolded immunoglobulin light chains. Overproduction of misfolded light chains results in both soluble, a... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) PT (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) GR (Trial now transitioned) NL (Trial now transitioned) IT (Trial now transitioned) IE (Trial now transitioned) BE (Trial now transitioned) AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000312-28 | Sponsor Protocol Number: P170901J | Start Date*: 2019-12-18 |
Sponsor Name:APHP / DRCI | ||
Full Title: Extending time without diabetes after bariatric surgery: a randomized controlled trial comparing the metformin addition or not to standard care | ||
Medical condition: Type 2 Diabetes complete remission after Bariatric surgery under antidiabetic drug | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001306-35 | Sponsor Protocol Number: APHP200394 | Start Date*: 2020-04-05 |
Sponsor Name:DRCI APHP | ||
Full Title: Protective role of inhaled steroids for COVID-19 infection | ||
Medical condition: COVID-19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024595-26 | Sponsor Protocol Number: 287-11-201 | Start Date*: 2011-10-27 |
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | ||
Full Title: Phase 2 Placebo-controlled Double-blind Trial of Dasatinib Added to Gemcitabine for Subjects with Locally-advanced Pancreatic Cancer | ||
Medical condition: Locally-advanced Pancreatic Adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) HU (Completed) GB (Completed) AT (Completed) DE (Completed) CZ (Completed) IE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003176-12 | Sponsor Protocol Number: A-93-52030-279 | Start Date*: 2014-08-27 | |||||||||||
Sponsor Name:IPSEN S.p.A | |||||||||||||
Full Title: A PHASE II, MULTICENTRE, RANDOMIZED CONTROLLED STUDY EVALUATING THE QUALITY OF LIFE IN PATIENTS WITH INOPERABLE MALIGNANT BOWEL OBSTRUCTION TREATED WITH LANREOTIDE AUTOGEL 120 MG IN COMBINATION WIT... | |||||||||||||
Medical condition: Inoperable malignant bowel obstruction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015659-26 | Sponsor Protocol Number: 2009-015659-26 | Start Date*: 2010-01-22 | |||||||||||||||||||||
Sponsor Name:Karolinska Institutet | |||||||||||||||||||||||
Full Title: Cortical and hormonal stress responses to pain management with morphine in standard clinical dosage | |||||||||||||||||||||||
Medical condition: Neonatal pain | |||||||||||||||||||||||
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Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022960-10 | Sponsor Protocol Number: CVC-202 | Start Date*: 2011-03-30 | |||||||||||
Sponsor Name:ChronTech Pharma AB | |||||||||||||
Full Title: A Phase II Open-Label, Randomized, Parallel group, Safety, Tolerability and Efficacy Study of i.m. Administered CHRONVAC-C in Combination with Electroporation followed by Standard of Care in Chroni... | |||||||||||||
Medical condition: Treatment of chronic infections caused by hepatitis C virus genotype 1 strains | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002998-20 | Sponsor Protocol Number: UNOLE0626 | Start Date*: 2017-10-04 |
Sponsor Name:University of Leicester | ||
Full Title: Effectiveness and cost of integrating a protocol with use of liraglutide 3.0mg into an obesity service (STRIVE Study) | ||
Medical condition: Obesity | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2012-002604-41 | Sponsor Protocol Number: WP6-282512 | Start Date*: 2014-01-31 |
Sponsor Name:University Medical Centre Utrech | ||
Full Title: RGNOSIS: Ecological Effects of Decolonisation Strategies in Intensive Care | ||
Medical condition: Colonisation and Infection with (multi drug resistant) Gram negative bacteria in ICU patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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