- Trials with a EudraCT protocol (10,062)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
10,062 result(s) found.
Displaying page 1 of 504.
| EudraCT Number: 2006-000653-22 | Sponsor Protocol Number: GART1013 | Start Date*: 2006-07-26 | |||||||||||
| Sponsor Name:Moorfields Eye Hospital | |||||||||||||
| Full Title: The UK Glaucoma Treatment Study | |||||||||||||
| Medical condition: Primary open-angle Glaucoma Pseudoexfoliation Glaucoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-007225-39 | Sponsor Protocol Number: CareRA | Start Date*: 2009-01-06 | |||||||||||
| Sponsor Name:University Hospitals Leuven | |||||||||||||
| Full Title: A 2 year prospective multicentre randomised controlled trial comparing effectiveness in daily practice of different treatment strategies for early RA | |||||||||||||
| Medical condition: early active Rheumatoid Arthritis, previously untreated with DMARDS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001795-19 | Sponsor Protocol Number: Uni-Koeln-1341 | Start Date*: 2012-09-13 |
| Sponsor Name:University of Cologne | ||
| Full Title: STATIN RECAPTURE THERAPY BEFORE CORONARY ARTERY BYPASS GRAFTING (ACRONYM: START-CABG TRIAL) | ||
| Medical condition: Patients on a long term statin therapy with established coronary artery disease (CAD) scheduled for isolated surgical myocardial revascularisation (i.e. CABG) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000309-60 | Sponsor Protocol Number: 120101 | Start Date*: 2016-03-30 | |||||||||||
| Sponsor Name:Göteborgs universitet | |||||||||||||
| Full Title: Biochemical and neuropsychological effects on Premenstrual Dysphoric Disorder after acute administration of escitalopram | |||||||||||||
| Medical condition: Premenstrual Dysphoric Disorder | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001722-25 | Sponsor Protocol Number: ZonMw80-83600-98-10226 | Start Date*: 2013-08-27 | |||||||||||
| Sponsor Name:VU University Medical Center | |||||||||||||
| Full Title: Cholinesterase inhibitors to slow progression of visual hallucinations in Parkinson’s disease: a multi-center placebo-controlled trial (CHEVAL) | |||||||||||||
| Medical condition: Parkinson's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003488-71 | Sponsor Protocol Number: OVG-2013/04 | Start Date*: 2013-12-12 |
| Sponsor Name:University of Oxford | ||
| Full Title: A pilot study of the impact of BCG administration on the immunogenicity of serogroup C meningococcal conjugate vaccine in healthy infants | ||
| Medical condition: Vaccine responses | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-004108-20 | Sponsor Protocol Number: UMCN-AKF13.05 | Start Date*: 2014-03-17 | ||||||||||||||||
| Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
| Full Title: Improving the tolerability of the oral targeted anti-cancer drug pazopanib by food intake (DIET) | ||||||||||||||||||
| Medical condition: Patients who are treated or will be treated with pazopanib. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-020841-29 | Sponsor Protocol Number: ADAPT | Start Date*: 2011-07-07 | ||||||||||||||||
| Sponsor Name:King`s College London [...] | ||||||||||||||||||
| Full Title: The role of anti-IgE (omalizumab) in the management of severe recalcitrant paediatric atopic eczema | ||||||||||||||||||
| Medical condition: Severe eczema in children | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-001223-31 | Sponsor Protocol Number: KAISII | Start Date*: 2016-10-11 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Incidence of Invasive Fungal Disease in Patients receiving Immunosuppressive Therapy, Intensive Chemotherapy or Reduced Intensity Haematopoietic Stem Cell Transplantation on Posaconazole Prophylaxis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Aplastic Anaemia, Myelodysplastic syndromes, Acute Myeloid Leukaemia undergoing immunosuppression therapy, high dose chemotherapy or reduced intensity stem cell transplantation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2015-002416-33 | Sponsor Protocol Number: GLARGL07667 | Start Date*: 2016-02-15 | |||||||||||
| Sponsor Name:sanofi-aventis France | |||||||||||||
| Full Title: An interventional, Open-label, single-arm, multicenter, 24 Weeks phase 4 study assessing the Efficacy and Safety of Toujeo in patients with Type 2 Diabetes inadequately controlled with Basal Insulin | |||||||||||||
| Medical condition: Type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001440-18 | Sponsor Protocol Number: IACI2016 | Start Date*: 2018-05-30 |
| Sponsor Name:university medical center utrecht | ||
| Full Title: Pharmacokinetic interactions between ivacaftor and cytochrome P450 3A4 inhibitors in cystic fibrosis patients and healthy controls | ||
| Medical condition: cystic fibrosis and healthy subjects | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002061-29 | Sponsor Protocol Number: 08227 | Start Date*: 2016-03-21 | |||||||||||
| Sponsor Name:Consorci Sanitari de Terrassa | |||||||||||||
| Full Title: Prospective randomized clinical trial comparing the effect of vaginal misoprostol synchronously with supracervical ball, versus only vaginal misoprostol for induction of labor. | |||||||||||||
| Medical condition: Pegnant women with a term singleton pregnancy, cephalic presentation, reassuring fetal heart rate pattern, intact membranes and an unfavorable cervix (Bishop score less than 6), admitted to our ins... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000238-23 | Sponsor Protocol Number: ExeBAT01 | Start Date*: 2016-08-09 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: The effect of Exenatide on brown adipose tissue activity and energy expenditure in healthy young men | ||
| Medical condition: Healthy volunteers, intended indications: obesity and dyslipidemia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-001264-11 | Sponsor Protocol Number: UMCM-2016EPI05 | Start Date*: 2016-09-07 |
| Sponsor Name:University Medical Center of the Johannes Gutenberg-University Mainz | ||
| Full Title: A phase IV, single-center, randomized, double-blind, placebo-controlled, parallel group study on the effects of empagliflozin on left ventricular diastolic function compared to usual care in indivi... | ||
| Medical condition: Poorly controlled type 2 diabetes mellitus in adults | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000608-14 | Sponsor Protocol Number: 1.0/170119 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Tartu University Hospital | ||
| Full Title: Prospective validation of individualized Bayesian dose optimization tool DosOpt for Vancomycin treatment in neonates. | ||
| Medical condition: In neonatal population wide inter-and intra-individual variability of pharmacokinetics makes extremely difficult to ensure optimal exposure of vancomycin with standard regimens. On average >50% of ... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
| Trial protocol: EE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000608-27 | Sponsor Protocol Number: ProtokolSB2 | Start Date*: 2016-04-05 | |||||||||||||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
| Full Title: The effect of subsartorial saphenous block on postoperative pain following major ankle and hind foot surgery | |||||||||||||||||||||||
| Medical condition: Post-operative pain after four types of major ankle and hind foot surgery: (1) total ankle arthroplasty, (2) ankle arthrodesis, (3) subtalar arthrodesis or (4) triple arthrodesis | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2016-000473-20 | Sponsor Protocol Number: CLCZ696B3402 | Start Date*: 2016-08-18 | |||||||||||
| Sponsor Name:Novartis Pharma services AG | |||||||||||||
| Full Title: A prospective evaluation of natriuretic peptide based referral of CHF patients in primary care | |||||||||||||
| Medical condition: Chronic heart failure with reduced ejection fraction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003486-17 | Sponsor Protocol Number: 9-VPH-MVIH | Start Date*: 2020-02-11 |
| Sponsor Name:CARMEN HIDALGO TENORIO | ||
| Full Title: Immunogenicity and safety of a 9-valent human papillomavirus vaccine in HIV-positive women | ||
| Medical condition: New infection and lesions of papillomavirus in HIV-infected women | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000605-20 | Sponsor Protocol Number: FFIS/2017/01/SLT | Start Date*: 2017-07-26 |
| Sponsor Name:Fundación para la Formación e Investigación Sanitarias de la Región de Murcia | ||
| Full Title: PERIPHERAL TRANSCUTANEOUS NEUROMODULATION OF THE POST-TIBIAL NERVE (T-PTNS) FOR SOLIFENACIN 10mg. IN THE TREATMENT OF HYPERACTIVE BLADDER SYNDROME: NON-INFERIORITY PHASE IV RANDOMIZED CLINICAL TRIAL | ||
| Medical condition: Overactive Bladder Syndrome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000502-11 | Sponsor Protocol Number: EKOS-12 | Start Date*: 2016-07-21 |
| Sponsor Name:EKOS Corporation | ||
| Full Title: Study of the Optimum Duration of Acoustic Pulse Thrombolysis (APT) Procedure in the Treatment of Acute Submassive Pulmonary Embolism (OPTALYSE PE). | ||
| Medical condition: Submassive pulmonary embolism | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
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