- Trials with a EudraCT protocol (51)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
51 result(s) found for: Reducing Agents.
Displaying page 1 of 3.
EudraCT Number: 2022-002741-18 | Sponsor Protocol Number: GS-US-611-6273 | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of GS-5245 for the Treatment of COVID-19 in Participants With High-Risk for Disease Progression | |||||||||||||
Medical condition: Coronavirus disease 2019 (COVID-19) in patients who have a high risk of developing serious or severe illness | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Ongoing) BG (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000046-19 | Sponsor Protocol Number: RIVAROXHFA3001/BAY59-7939/16302 | Start Date*: 2013-08-23 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Event-driven, Multicenter Study Comparing the Efficacy and Safety of Oral Rivaroxaban with Placebo for Reducing the Risk of Death, Myocardial Infarction or Stroke in Sub... | |||||||||||||
Medical condition: Prevention of death, heart attack and stroke in patients with chronic heart failure and significant coronary artery disease following a hospitalization for exacerbation of heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) NL (Completed) BG (Completed) PL (Completed) HU (Completed) SE (Completed) IT (Completed) GB (Completed) EE (Completed) LT (Completed) PT (Completed) DK (Completed) LV (Completed) SK (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000487-11 | Sponsor Protocol Number: CRFB002D2201 | Start Date*: 2005-09-30 |
Sponsor Name:Novartis Pharma Service AG | ||
Full Title: A randomized, double-masked, multicenter, phase II study assessing the safety and efficacy of two concentrations of ranibizumab (intravitreal injections) compared with non-treatment control for the... | ||
Medical condition: Male and female patients >18 years of age with either type 1 or type 2 diabetes mellitus with stable HbA1c levels between 6.5 and 10% and diabetic macular edema with center involvement in at least ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) DK (Completed) GB (Completed) AT (Completed) ES (Completed) IT (Completed) PT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001054-84 | Sponsor Protocol Number: 2004/W/GI/02 | Start Date*: 2005-02-16 |
Sponsor Name:NHS Lothian- University Hospitals Division | ||
Full Title: A comparison of the efficacy of dietary hydroxypropylcellulose and questran as therapeutic agents in bile acid induced diarrhoea | ||
Medical condition: these patients will have bile acid induced diarrhoea identified by an increased serum 7a-OH-cholestenone. and will have a history of one of 1. ileal resection 2. idiopathic bile acid diarrhoea.3. ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003612-30 | Sponsor Protocol Number: 0904HELIOX | Start Date*: 2005-11-23 |
Sponsor Name:Barts and the London NHS Trust | ||
Full Title: A comparison of Helium-oxygen mixture (Heliox) with an oxygen-air mixture in reducing the work of breathing during weaning from mechanical ventilation. | ||
Medical condition: Patients admitted to the intensive care unit who are in the recovery phase of their illness and are weaning from mechanical ventilation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004260-22 | Sponsor Protocol Number: ELFIN01 | Start Date*: 2013-08-28 |
Sponsor Name:University of Oxford | ||
Full Title: A multi-centre randomised placebo-controlled trial of prophylactic enteral lactoferrin supplementation to prevent late-onset invasive infection in very preterm infants. | ||
Medical condition: Late onset invasive infection in very preterm infants | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001539-10 | Sponsor Protocol Number: UX007-CL302 | Start Date*: 2022-12-27 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceutical Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Multicenter Study to Determine the Effect of Triheptanoin Compared with Even-chain, Medium-chain Triglycerides (MCT) on Major Clinical Events (MCEs) in Pediatric Patient... | |||||||||||||
Medical condition: Long-chain Fatty Acid Oxidation Disorders (LC-FAOD) | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Ongoing) CZ (Ongoing) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002349-23 | Sponsor Protocol Number: 8232-CL-0004 | Start Date*: 2015-01-26 | |||||||||||
Sponsor Name:Astellas Pharma Europe BV (APEB) | |||||||||||||
Full Title: A Phase 2, Double-Blind, Randomized, Placebo Controlled Study to Evaluate the Efficacy and Safety of ASP8232 as Add-On Therapy to Angiotensin Converting Enzyme inhibitor (ACEi) or Angiotensin Recep... | |||||||||||||
Medical condition: Diabetic nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (Completed) HU (Completed) CZ (Completed) DE (Completed) BE (Completed) IT (Completed) NL (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004889-34 | Sponsor Protocol Number: NN7415-4311 | Start Date*: 2019-10-07 | ||||||||||||||||
Sponsor Name:Novo Nordisk A/S | ||||||||||||||||||
Full Title: Efficacy and Safety of Concizumab prophylaxis in patients with haemophilia A or B with inhibitors | ||||||||||||||||||
Medical condition: Haemophilia A with inhibitors Haemophilia B with inhibitors | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: DK (Trial now transitioned) SE (Trial now transitioned) AT (Completed) FR (Ongoing) PT (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) SK (Completed) NO (Ongoing) BG (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) HR (Ongoing) IT (Restarted) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004204-39 | Sponsor Protocol Number: 108701 | Start Date*: 2007-02-01 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: A randomized, open label, multicentre study to compare the pharmaco-economic implications of an analgesia based regimen with remifentanil and a conventional sedation based regimen using propofol in... | |||||||||||||
Medical condition: Medical and post surgical ICU patient requiring analgesia and sedation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001831-73 | Sponsor Protocol Number: REDOXS© | Start Date*: 2009-03-12 |
Sponsor Name:Kingston General Hospital, Queen's University of Kingston | ||
Full Title: REducing Deaths due to OXidative Stress The REDOXS© Study A 2×2 factorial randomized trial of glutamine and antioxidant supplementation in critically ill patients | ||
Medical condition: Critically ill patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002472-99 | Sponsor Protocol Number: EVT302/3009 | Start Date*: 2008-08-12 |
Sponsor Name:Evotec Neurosciences GmbH | ||
Full Title: A phase II multicenter, randomised, double-blind, parallel group, placebo-controlled, study to evaluate the effectiveness of EVT 302 in smoking cessation, effect on its own and in combination with ... | ||
Medical condition: Male or female subjects who are chronic smokers, but motivated to quit smoking will be recruited. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004191-35 | Sponsor Protocol Number: GLYCO-1B | Start Date*: 2019-04-12 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Evaluation of the safety and efficacy of administration of Empagliflozin in a new treatment for neutropenia in patients with Glycogen Storage Disease type 1b (GSD1b) and G6PC3 deficiency. | ||
Medical condition: (1) Severe Congenital Neutropenia type 4 (SNC4) due to a deficiency in G6PC3, a phosphatase of the endoplasmic also known a Ubiquitous glucose-6-phosphatase and (2) the neutropenia in Glycogen Sto... | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000225-51 | Sponsor Protocol Number: ITP-NODAT | Start Date*: 2012-11-21 |
Sponsor Name:Fundació Institut Mar d'investigacions Mediques | ||
Full Title: Insulin Therapy for the Prevention of New Onset Diabetes after Transplantation (ITP-NODAT) Prospective Study in Non-Diabetic De Novo Kidney Transplant Recipients | ||
Medical condition: Previously non-diabetic end stage renal disease patients undergoing kidney transplantation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021718-41 | Sponsor Protocol Number: 214868-004-03 | Start Date*: 2011-03-03 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: A Pilot, Multicenter, Double-blind, Placebo-controlled, Dose-escalation Study of the Safety and Efficacy of AGN-214868 in Patients with Idiopathic Overactive Bladder and Urinary Incontinence | |||||||||||||
Medical condition: To evaluate the safety and efficacy of AGN-214868 compared with placebo in the treatment of patients with idiopathic overactive bladder (IOAB) and urinary incontinence. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001134-11 | Sponsor Protocol Number: 1305-0023 | Start Date*: 2022-11-22 | |||||||||||
Sponsor Name:Boehringer Ingelheim International GmbH | |||||||||||||
Full Title: A double blind, randomized, placebo-controlled trial evaluating the efficacy and safety of BI 1015550 over at least 52 weeks in patients with Progressive Fibrosing Interstitial Lung Diseases (PF-ILDs) | |||||||||||||
Medical condition: Progressive Fibrosing Interstitial Lung Diseases (PF-ILDs) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Ongoing) ES (Ongoing) AT (Ongoing) DE (Ongoing) NO (Ongoing) EE (Ongoing) FI (Ongoing) SE (Ongoing) PT (Ongoing) NL (Ongoing) HU (Ongoing) DK (Ongoing) GR (Ongoing) IT (Ongoing) HR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001419-29 | Sponsor Protocol Number: HRVCTA1 | Start Date*: 2011-05-05 | |||||||||||
Sponsor Name:Universitätsklinik für Radiodiagnostik | |||||||||||||
Full Title: Influence of iodinated contrast agents on heart rate variation and diagnostic image quality during CT angiography of the coronary arteries | |||||||||||||
Medical condition: CT angiography of the coronary arteries | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000319-21 | Sponsor Protocol Number: ClonDO | Start Date*: 2021-12-20 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Treating Nightmares in Posttraumatic Stress Disorder with the α-adrenergic Agents Clonidine and Doxazosin: A Randomized-Controlled Feasibility Study (ClonDoTrial) | ||
Medical condition: Posttraumatic Stress Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001898-25 | Sponsor Protocol Number: DAR-311 | Start Date*: 2006-09-21 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: DORADO - Fixed Doses of Darusentan as Compared to Placebo in Resistant Hypertension A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Parallel Group Study to Evaluate the Effica... | |||||||||||||
Medical condition: Resistant hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005330-20 | Sponsor Protocol Number: WA20495 | Start Date*: 2007-06-07 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A randomized, double-blind, parallel group, international study to evaluate the safety and efficacy of ocrelizumab compared to placebo in patients with active rheumatoid arthritis who have an in... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) HU (Completed) ES (Temporarily Halted) CZ (Completed) NL (Completed) SI (Completed) SE (Completed) IT (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
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