- Trials with a EudraCT protocol (38,658)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
38,658 result(s) found for: decitabine OR 2'-.
Displaying page 42 of 1,933.
| EudraCT Number: 2013-000225-30 | Sponsor Protocol Number: DMA-Clin-199-2013-001 | Start Date*: 2013-04-12 | |||||||||||
| Sponsor Name:DiaMedica USA Inc. | |||||||||||||
| Full Title: A DOUBLE-BLINDED, PLACEBO-CONTROLLED, SINGLE DOSE AND MULTIPLE-DOSE STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS AND PROOF OF CONCEPT OF DM-199 IN HEALTHY SUBJECTS... | |||||||||||||
| Medical condition: Diabetes Mellitus type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005344-95 | Sponsor Protocol Number: 3004 | Start Date*: 2012-06-15 |
| Sponsor Name:Steno Diabetes Center | ||
| Full Title: Time course of the blood pressure lowering effect of liraglutide therapy in type 2 diabetes | ||
| Medical condition: type 2 diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004709-42 | Sponsor Protocol Number: NL63792.099.17 | Start Date*: 2018-04-24 |
| Sponsor Name:Martini Hospital | ||
| Full Title: An open-label randomised cross-over study to evaluate the albuminuria lowering effect of dapagliflozin, exenatide and their combination in patients with type 2 diabetes | ||
| Medical condition: Type 2 diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004793-34 | Sponsor Protocol Number: P171103J | Start Date*: 2018-07-10 |
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
| Full Title: 68Ga-DOTATATE PET-CTA imaging for the early detection of progressing coronary atherosclerosis | ||
| Medical condition: Patients with coronary atherosclerosis without significant myocardial ischemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-003177-14 | Sponsor Protocol Number: IBUPAR-Trial | Start Date*: 2016-04-06 |
| Sponsor Name: | ||
| Full Title: Paracetamol versus ibuprofen in preterm infants with a hemodynamically significant patent ductus arteriosus: a randomized clinical trial. | ||
| Medical condition: Persistent ductus arteriosus haemodynamically significant | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023231-42 | Sponsor Protocol Number: I1R-MC-GLBG | Start Date*: 2011-04-04 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 2b Study of LY2409021 in Patients with Type 2 Diabetes Mellitus | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SK (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001455-42 | Sponsor Protocol Number: NL56309.091.16 | Start Date*: 2016-04-20 |
| Sponsor Name:Radboud Universitair Medisch Centrum | ||
| Full Title: The influence of metformin and a hypocaloric diet on thyroid radioactive iodide uptake in healthy volunteers: a pilot study | ||
| Medical condition: physiological thyroid function in terms of thyroid iodide uptake and thyroid hormone production knowledge can be extrapolated for treatment of thyroid diseases such as hyperthyroidism and thyroid ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-000813-63 | Sponsor Protocol Number: TACs | Start Date*: 2016-04-06 |
| Sponsor Name:Universitair Ziekenhuis Brussel | ||
| Full Title: Comparative doubleblind study with prilocaine 2 % and 2-chloroprocaine for elective caesarean section. | ||
| Medical condition: Healthy pregnant women undergoing a elective caesarean section with an uncomplicated pregnancy of a singleton, "full-term", all between 18-40 y (ASAI-II) through combined spinal and epidural approach. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-001176-30 | Sponsor Protocol Number: 20167169 | Start Date*: 2016-06-15 |
| Sponsor Name:Clinical Research Institute, HUCH Ltd. | ||
| Full Title: Effects of PCSK9 inhibition by Evolocumab on postprandial lipid metabolism in type 2 diabetes | ||
| Medical condition: type 2 diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002031-24 | Sponsor Protocol Number: HAM005 | Start Date*: 2006-06-14 |
| Sponsor Name:Imperial College | ||
| Full Title: The HAM Ciclosporin Study: An observational trial of therapy in early or progressing HAM/TSP | ||
| Medical condition: HTLV-I-associated myelopathy | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-002010-19 | Sponsor Protocol Number: TASC07 | Start Date*: 2007-10-15 |
| Sponsor Name:University of Dundee | ||
| Full Title: The TASCFORCE Project: Tayside Screening For risk of Cardiac Events and the effect of statin on risk reduction (as evidenced by change in LV mass) | ||
| Medical condition: The aim of this study is to validate MRI as a screening tool for detection of early signs of heart disease. Those thought to be at the highest risk of developing cardiovascular disease will be rand... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-010145-31 | Sponsor Protocol Number: M48P3E1 | Start Date*: 2009-04-27 |
| Sponsor Name:Novartis Vaccines and Diagnostics GmbH & Co. KG | ||
| Full Title: A phase IV, open-label, multi-center follow-up study to determine the persistence of tick-borne encephalitis (TBE)-specific antibody responses among children and adolescents previously immunized ag... | ||
| Medical condition: No medical condition, healthy volunteers will be recruited. (In this study the status of antibody titers against tick borne encephalitis will be investigated in healthy subjects who have received ... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-002744-14 | Sponsor Protocol Number: PRILPLEXUS1%-1.5% | Start Date*: 2015-12-23 |
| Sponsor Name:Universitair Ziekenhuis Brussel | ||
| Full Title: Comparative study with prilocaine 1% and prilocaine 1.5% for ultrasound guided axillary brachial plexus blockade | ||
| Medical condition: - Onset of sensory and motor block - Quality and duration of the block - Influence of prilocaine on methemoglobinemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001251-41 | Sponsor Protocol Number: P20/05 | Start Date*: 2020-04-17 | |||||||||||
| Sponsor Name:CH de Versailles | |||||||||||||
| Full Title: A PROOF OF CONCEPT STUDY TESTING THE VALUE OF IMATINIB IN PREVENTION OF COVID-19 IN AGED PATIENTS. | |||||||||||||
| Medical condition: Aged patients at risk of COVID-19 infection | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002085-63 | Sponsor Protocol Number: LIDO-CLOR | Start Date*: 2008-05-13 | |||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
| Full Title: TREATMENT OF CHRONIC PAIN BY NEUROMODULATION WITH LOCAL ANESTHETIC (NEURALTHERAPY) IN OPERATED AND / OR IRRADIATED PATIENTS FOR HEAD AND NECK, BREST AND, INTRATHROCIC NEOPLASM | |||||||||||||
| Medical condition: CHRONIC PAIN IN OPERATED AND / OR IRRADIATED PATIENTS FOR HEAD AND NECK, BREST AND, INTRATHROCIC NEOPLASM | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001165-88 | Sponsor Protocol Number: ITCA650-CLP-203 | Start Date*: 2017-06-22 | ||||||||||||||||
| Sponsor Name:Intarcia Therapeutics, Inc. | ||||||||||||||||||
| Full Title: A Phase 3b, Randomized, Active Comparator, Open-label, Multicenter Study to Compare the Efficacy, Safety, and Tolerability of ITCA 650 to Empagliflozin and to Glimepiride as Add-on Therapy to Metfo... | ||||||||||||||||||
| Medical condition: Type 2 diabetes | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Prematurely Ended) GB (Prematurely Ended) NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-002391-97 | Sponsor Protocol Number: PML_DOC_0802 | Start Date*: 2008-06-19 |
| Sponsor Name:University Hospital Antwerp; Department Respiratory Medicine | ||
| Full Title: Open-label, prospective study to assess the effects of formoterol and beclometasone dipropionate combination therapy on central and peripheral airway dimensions in asthmatic patients | ||
| Medical condition: Asthma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020018-27 | Sponsor Protocol Number: Dbox2008/01978 | Start Date*: 2012-04-19 |
| Sponsor Name:Tameside Hospital NHS Foundation Trust | ||
| Full Title: Effect of Testosterone on endothelial function and Microcirculation in Type 2 Diabetic patients with Hypoganadism. | ||
| Medical condition: Hypogonadism and erectile dysfunction in patients with type 2 diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004183-21 | Sponsor Protocol Number: 2858 | Start Date*: 2013-01-25 |
| Sponsor Name:North Bristol NHS Trust | ||
| Full Title: A randomized, double blind, placebo controlled, cross over trial of Melatonin for the treatment of nocturia in adults with progressive multiple sclerosis, with an open label, single-arm extension s... | ||
| Medical condition: Nocturia; Multiple Sclerosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004533-13 | Sponsor Protocol Number: EFC13470 | Start Date*: 2015-07-17 | |||||||||||
| Sponsor Name:Sanofi-aventis recherche & développement | |||||||||||||
| Full Title: A 21-Week, Open-label, Randomized, Controlled, Parallel-group, Multi-center Study Evaluating the Efficacy and Safety of HOE901-U300 Administered According to a Device-Supported Treat-to-target Regi... | |||||||||||||
| Medical condition: Type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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