- Trials with a EudraCT protocol (8,950)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8,950 result(s) found.
Displaying page 230 of 448.
| EudraCT Number: 2016-003575-21 | Sponsor Protocol Number: | Start Date*: 2017-07-25 | |||||||||||
| Sponsor Name:MRC Clinical Trials Unit at UCL | |||||||||||||
| Full Title: A multicentre, 48 week randomised controlled factorial trial of adding maraviroc and/or metformin for hepatic steatosis in HIV-1-infected adults on combination antiretroviral therapy. | |||||||||||||
| Medical condition: Hepatic steatosis in adults with chronic HIV-1 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021165-76 | Sponsor Protocol Number: LU2006 | Start Date*: 2011-09-19 | |||||||||||
| Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: STOMP: Small cell lung cancer Trial of Olaparib (AZD2281) as Maintenance Programme: a randomised, double blind, multicentre phase II trial | |||||||||||||
| Medical condition: Small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-003420-33 | Sponsor Protocol Number: NL78216 | Start Date*: 2021-12-13 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Tacrolimus versus mycophenolate for AutoImmune hepatitis patients with incompLete response On first line therapy: a Randomized trial (TAILOR study) | ||
| Medical condition: Autoimmune hepatitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001398-22 | Sponsor Protocol Number: SOLTI-1910 | Start Date*: 2021-12-28 |
| Sponsor Name:SOLTI | ||
| Full Title: Predicting olaparib sensitivity in patients with unresectable locally advanced/metastatic HER2-negative breast cancer with BRCA1, BRCA2, PALB2, RAD51C or RAD51D mutations or RAD51-foci low test: RA... | ||
| Medical condition: Pre and post-menopausal women and men with unresectable locally advanced or metastatic triple negative breast cancer (TNBC) or ET ±CDK4/6-resistant hormonal receptor positive and HER2-negative (HR+... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000265-33 | Sponsor Protocol Number: 3000LM | Start Date*: 2021-02-25 |
| Sponsor Name:The Rotterdam Eye Hospital | ||
| Full Title: Prospective study on safety and efficacy of gene therapy with voretigene neparvovec (Luxturna®) in patients with RPE65-associated inherited retinal degenerations | ||
| Medical condition: RPE65-associated inherited retinal degeneration | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004938-11 | Sponsor Protocol Number: PI-GR-21-2386 | Start Date*: 2021-12-21 |
| Sponsor Name:Hospital Clínico Universitario de Valladolid | ||
| Full Title: Prevention of cardiac surgery-associated acute kidney injury through the use of sodium-glucose cotransporter 2 inhibitors | ||
| Medical condition: Cardiac surgery-associated acute kidney injury | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001872-12 | Sponsor Protocol Number: CL-N-LTX-III/08-ESP/19 | Start Date*: 2021-12-28 | |||||||||||||||||||||
| Sponsor Name:Dr. Franz Köhler Chemie GmbH | |||||||||||||||||||||||
| Full Title: A Prospective, randomized, single blind, multicenter Phase III study on organ preservation with Custodiol-N solution compared with Custodiol solution in liver transplantation | |||||||||||||||||||||||
| Medical condition: Liver transplantation. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2021-001827-41 | Sponsor Protocol Number: PI2020_843_0094 | Start Date*: 2021-06-11 |
| Sponsor Name:CHU Amiens-Picardie | ||
| Full Title: Evaluation of the early use of norepinephrine in major abdominal surgery on postoperative organ dysfunction | ||
| Medical condition: major abdominal surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000370-10 | Sponsor Protocol Number: POLEMCCR4673 | Start Date*: 2018-05-09 | |||||||||||
| Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
| Full Title: Avelumab plus fluoropyrimidine-based chemotherapy as adjuvant treatment for stage III dMMR or POLE exonuclease domain mutant colon cancer: A phase III randomised study. | |||||||||||||
| Medical condition: Colon cancer stage III | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000196-27 | Sponsor Protocol Number: 9744 | Start Date*: 2015-07-28 | |||||||||||
| Sponsor Name:QMUL and Bart's Health NHS trust | |||||||||||||
| Full Title: Tendinopathy treatment effects and mechanisms 1 (TEAM 1): A randomised clinical trial of eccentric loading, high volume injection and shock wave therapy for Achilles tendinopathy. | |||||||||||||
| Medical condition: Achilles tendinopathy | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003203-35 | Sponsor Protocol Number: VP-C21-004 | Start Date*: 2019-12-13 | ||||||||||||||||
| Sponsor Name:Vicore Pharma AB | ||||||||||||||||||
| Full Title: A Phase 2, single-center, randomised, double-blind, placebo-controlled, cross-over, cold challenge study investigating the effect of C21 on cold-induced vasoconstriction in subjects with Raynaud’s ... | ||||||||||||||||||
| Medical condition: Systemic sclerosis (SSc) Raynaud’s phenomenon (RP) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-005207-32 | Sponsor Protocol Number: RG_11-187 | Start Date*: 2012-06-08 | |||||||||||
| Sponsor Name:The University of Birmingham | |||||||||||||
| Full Title: Phase II Randomised Trial of 5-Azacitidine versus 5-Azacitidine in combination with Vorinostat in patients with Relapsed Acute Myeloid Leukaemia ineligible for Intensive Chemotherapy | |||||||||||||
| Medical condition: Haematological Malignancy - Acute Myeloid Leukaemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001485-17 | Sponsor Protocol Number: GS-US-432-4097 | Start Date*: 2017-08-15 | |||||||||||||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||||||||||||
| Full Title: A Phase 2, Randomized, Placebo-Controlled Trial Evaluating the Efficacy and Safety of Filgotinib in Subjects with Active Non-Infectious Uveitis | |||||||||||||||||||||||
| Medical condition: Non-infectious Uveitis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2021-003847-10 | Sponsor Protocol Number: SHORTENII | Start Date*: 2022-01-12 | ||||||||||||||||
| Sponsor Name:Fundación Pública Andaluza para la Gestión de la Investigación en Salud de Sevilla (FISEVI) | ||||||||||||||||||
| Full Title: Efficacy and safety of 7 versus 14 days of antibiotic treatment for Pseudomonas aeruginosa bacteraemia: a multicentre, randomized clinical trial (SHORTEN-2) with a DOOR/RADAR analysis | ||||||||||||||||||
| Medical condition: Adult patients with bloodstream infections produced by Pseudomonas aeruginosa. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-000507-20 | Sponsor Protocol Number: CIRCULATE-SPAIN-01 | Start Date*: 2022-01-12 | ||||||||||||||||
| Sponsor Name:Instituto de Investigación Sanitaria INCLIVA | ||||||||||||||||||
| Full Title: Phase II randomized trial to assess the effect of intensive vs standard adjuvant chemotherapy in localised colon cancer with circulating tumor DNA | ||||||||||||||||||
| Medical condition: Localised Colon Cancer (stage II-III) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-001069-20 | Sponsor Protocol Number: HIDROGUM21 | Start Date*: 2022-01-12 |
| Sponsor Name:Vall d'Hebron Hospital Universitari | ||
| Full Title: Tolerability and acceptance of two oral hydrocortisone compounding formulation for pediatrics | ||
| Medical condition: Adrenal hyperplasia or isolated primary adrenal insufficiency or panhypopituitarism (secondary or tertiary adrenal insufficiency) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003229-47 | Sponsor Protocol Number: KEEP-ON | Start Date*: 2022-01-12 | |||||||||||||||||||||
| Sponsor Name:Instituto de Investigación Sanitaria INCLIVA | |||||||||||||||||||||||
| Full Title: Phase III, multicenter, open-label, randomized clinical trial to evaluate efficacy of Sodium Zirconium Cyclosilicate (Lokelma) compared to standard of care to manage hyperkalemia in patients with c... | |||||||||||||||||||||||
| Medical condition: Hyperkalemia in patients with chronic kidney disease (CKD) and heart failure history | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2019-002744-24 | Sponsor Protocol Number: CLI-05993AA1-21 | Start Date*: 2020-02-13 |
| Sponsor Name:Chiesi Farmaceutici S.p.A. | ||
| Full Title: A phase IV, open label, multicentre, randomised, 2-way cross-over exploratory clinical trial comparing a fixed combination of beclometasone dipropionate plus formoterol fumarate plus glycopyrronium... | ||
| Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-003823-14 | Sponsor Protocol Number: CDCA-PK | Start Date*: 2021-11-16 |
| Sponsor Name:Amsterdam UMC | ||
| Full Title: Pharmacokinetic cross-over study of compounded chenodeoxycholic acid. | ||
| Medical condition: CTXCT | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000569-61 | Sponsor Protocol Number: CHUBX2016/27 | Start Date*: 2021-12-20 |
| Sponsor Name:CHU de Bordeaux | ||
| Full Title: Comparison of therapeutic strategies with Cholinesterase Inhibitors: stop or still (SOS) trial | ||
| Medical condition: Alzheimer disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
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