- Trials with a EudraCT protocol (542)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
542 result(s) found for: Active Monitoring.
Displaying page 8 of 28.
EudraCT Number: 2015-004173-32 | Sponsor Protocol Number: 1-10-72-164-15 | Start Date*: 2015-12-18 | |||||||||||
Sponsor Name:Department of Clinical Biochemestry, Aarhus University Hospital | |||||||||||||
Full Title: Personalized medicine: Administration of TNF-alpha inhibitor treatment due to serum concentration measuring. A randomized and investigator initiated study. | |||||||||||||
Medical condition: Rheumatic diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001054-57 | Sponsor Protocol Number: NL76562.100.21 | Start Date*: 2021-03-08 | |||||||||||
Sponsor Name:OLVG | |||||||||||||
Full Title: SARS-CoV-2 vaccination response in people living with HIV | |||||||||||||
Medical condition: COVID-19 vaccine response in people living with HIV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003932-26 | Sponsor Protocol Number: Ga-68-CCK2R | Start Date*: 2021-01-20 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Phase I/IIa study to evaluate the safety, tolerability, whole-body distribution, and preliminary diagnostic performance of a novel 68Ga-labelled minigastrin analogue in patients with advanced neuro... | ||
Medical condition: Advanced neuroendocrine tumours (NET), including medullary thyroid carcinoma (MTC), as well as gastroenteropancreatic and bronchopulmonary NET | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005407-24 | Sponsor Protocol Number: KKIKEM | Start Date*: 2015-02-27 |
Sponsor Name:IKEM | ||
Full Title: Effect of early administration of eplerenone in patients after acute myocardial infarction | ||
Medical condition: Verify the efficacy of early administration of eplerenone in relation to the development of pathological remodeling of the myocardium in patients after myocardial infarction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001784-27 | Sponsor Protocol Number: 2018/0419/HP | Start Date*: 2022-10-11 |
Sponsor Name:Direction de la Recherche Clinique et de l'Innovation - CHU de Rouen | ||
Full Title: Tolerance of intra-articular injection of autologous stromal vascular fraction for the treatment of rhizarthrosis | ||
Medical condition: Adults with a rhizarthrosis stage DELL 1 to 3 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003103-22 | Sponsor Protocol Number: BONSAI | Start Date*: 2017-11-28 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Advanced or Metastatic Collecting ducts renal cell carcinoma | |||||||||||||
Medical condition: Collecting Duct Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001926-25 | Sponsor Protocol Number: B300201316844 | Start Date*: 2013-09-23 |
Sponsor Name:Universitair Ziekenhuis Antwerpen | ||
Full Title: Sugammadex and the diaphragm: recovery of diaphragmatic function and neuromuscular blockade | ||
Medical condition: Residual neuromuscular blockade and diphragm fatigue | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002679-25 | Sponsor Protocol Number: S60420 | Start Date*: 2017-09-12 |
Sponsor Name:KU Leuven | ||
Full Title: Characterization of colonic motility patterns in different functional bowel disorders compared to health and their role in moving content | ||
Medical condition: Functional bowel disorders; irritable bowel syndrome (constipation, diarrhea and mixed), chronic constipation, and chronic diarrhea. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-000837-17 | Sponsor Protocol Number: NL80854.018.22 | Start Date*: 2022-12-07 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Subcutaneous vedolizumab drug de-escalation using therapeutic drug monitoring in inflammatory bowel disease: a randomized controlled pilot study | ||
Medical condition: Inflammatory bowel diseases (Crohn's disease, ulcerative colitis) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004420-30 | Sponsor Protocol Number: CL3-95008-002 | Start Date*: 2018-10-04 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Efficacy and safety of bumetanide oral liquid formulation in children aged from 2 to less than 7 years old with Autism Spectrum Disorder. A 6-month randomised, double-blind, placebo controlled mult... | |||||||||||||
Medical condition: Autism Spectrum Disorder (ASD) | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) ES (Prematurely Ended) NL (Not Authorised) HU (Completed) PT (Completed) PL (Prematurely Ended) IE (Prematurely Ended) CZ (Completed) SK (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003784-42 | Sponsor Protocol Number: RV-MM-PI-278 | Start Date*: 2008-11-24 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Dose-finding study of lenalidomide as maintenance therapy in multiple myeloma after allogeneic stem cell transplantation | |||||||||||||
Medical condition: Multiple Myeloma patients who received allogeneic stem cell transplantation (100 to 180 days ago) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002556-32 | Sponsor Protocol Number: ANTIC:6672 | Start Date*: 2013-09-05 | |||||||||||
Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Antibiotic treatment for intermittent bladder catheterisation: A randomised controlled trial of once daily prophylaxis (The AnTIC study) | |||||||||||||
Medical condition: Recurrent urinary tract infection in people who use intermittent bladder catheterisation. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003721-22 | Sponsor Protocol Number: A4091058 | Start Date*: 2016-01-14 | ||||||||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | ||||||||||||||||||
Full Title: A PHASE 3 RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED, MULTICENTER STUDY OF THE LONG-TERM SAFETY AND EFFICACY OF SUBCUTANEOUS ADMINISTRATION OF TANEZUMAB IN SUBJECTS WITH OSTEOARTHRITIS OF THE HIP ... | ||||||||||||||||||
Medical condition: Osteoarthritis of the hip or knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) SK (Completed) LT (Completed) HR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004152-10 | Sponsor Protocol Number: EMPATHY | Start Date*: 2020-01-30 | ||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||
Full Title: Evaluating the Short-Term Renal and Systemic Effects of SGLT2 Inhibition in Non-Diabetic Patients at Risk of Accelerated GFR Decline Because of Glomerular Hyperfiltration: a sequential OFF-ON-OFF S... | ||||||||||||||||||
Medical condition: Obesity Renal chronic disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003542-17 | Sponsor Protocol Number: CU-LATER | Start Date*: 2014-06-11 |
Sponsor Name:Charité Universitätsmedizin Berlin | ||
Full Title: A multi-center, randomized, double blind, dose escalating phase III study on the efficacy, safety and long term outcome of continuous vs. on demand treatment of chronic spontaneous urticaria with r... | ||
Medical condition: Chronic Spontaneous Urticaria | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2022-003526-50 | Sponsor Protocol Number: HACOL-ACS | Start Date*: 2023-05-09 | ||||||||||||||||
Sponsor Name:Hannover Medical School | ||||||||||||||||||
Full Title: A prospective, interventional, single-center, single-arm study to assess the effectiveness of Bempedoic acid to achieve LDL-cholesterol targets in patients following ST-elevation or Non-ST-elevatio... | ||||||||||||||||||
Medical condition: Patients following acute percutaneous coronary intervention for STEMI or NSTEMI insufficiently treated with high-intensity oral lipid lowering therapy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003532-68 | Sponsor Protocol Number: FIBCON | Start Date*: 2014-03-11 | ||||||||||||||||
Sponsor Name:Guy's and St Thomas NHS Foundation Trust | ||||||||||||||||||
Full Title: Fibrinogen concentrate supplementation in the management of bleeding during paediatric cardiopulmonary bypass: a phase 1B/2A, open label dose escalation study (Version 1.0, Jan 28, 2014) | ||||||||||||||||||
Medical condition: Neonates and infants who are at risk of mediastinal bleeding following cardiopulmonary bypass surgery for congenital heart disease | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-007346-63 | Sponsor Protocol Number: ALS-003-2008 | Start Date*: 2011-04-05 |
Sponsor Name:Alloksys Life Sciences B.V. | ||
Full Title: Reumap: An Open Label phase II study of Bovine Intestinal Alkaline Phosphatase (bIAP), An Inflammation modulating moiety, in RA patients | ||
Medical condition: Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Temporarily Halted) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003187-20 | Sponsor Protocol Number: | Start Date*: 2015-05-21 |
Sponsor Name:Barts Health NHS Trust | ||
Full Title: A multicentre double-blind randomised controlled trial to assess the clinical- and cost-effectiveness of facet-joint injections in selected patients with non-specific low back pain: a feasibility s... | ||
Medical condition: Non-specific low back pain of more than three months' duration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-004246-15 | Sponsor Protocol Number: CAIN457FDE04 | Start Date*: 2020-08-27 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 28-week, randomized, double-blind, active-controlled, multicenter study to evaluate the efficacy of subcutaneously administered secukinumab compared to ustekinumab in adult patients with psoriati... | |||||||||||||
Medical condition: Psoriatic arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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