- Trials with a EudraCT protocol (43,977)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
43,977 result(s) found.
Displaying page 1,786 of 2,199.
EudraCT Number: 2019-000972-40 | Sponsor Protocol Number: IM101-774 | Start Date*: 2020-06-09 | |||||||||||
Sponsor Name:Universitätsklinikum Freiburg | |||||||||||||
Full Title: Safety and Efficacy of abatacept (s.c.) in patients with CTLA4 insufficiency or LRBA deficiency | |||||||||||||
Medical condition: Patients with a molecular confirmed diagnosis of CTLA4 (cytotoxic T-lymphocyte-associated Protein 4) (haplo)-insufficiency or LRBA (Lipopolysaccharide-Responsive and Beige-like An¬chor) deficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003727-22 | Sponsor Protocol Number: CER13266 | Start Date*: 2015-05-26 | |||||||||||||||||||||
Sponsor Name:Geneva University Hospitals | |||||||||||||||||||||||
Full Title: A randomized controlled multicenter trial of a five day course of oral colistin and neomycin followed by restoration of the gut microbiota using fecal transplantation to eradicate intestinal carr... | |||||||||||||||||||||||
Medical condition: Intestinal colonization with extended-spectrum beta-lactamse or carbapenemase producing enterobacteriaceae | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000469-35 | Sponsor Protocol Number: CL03-ORY-1001SCLC | Start Date*: 2018-10-10 | |||||||||||
Sponsor Name:Oryzon Genomics S. A. | |||||||||||||
Full Title: A pilot study to assess the safety, tolerability, dose finding and efficacy ORY-1001 in combination with platinum-etoposide chemotherapy in patients with relapsed, extensive-stage disease small cel... | |||||||||||||
Medical condition: Relapsed, extended-stage disease small cell lung cancer (ED SCLC). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002978-36 | Sponsor Protocol Number: OVG2014/08 | Start Date*: 2015-01-26 | |||||||||||
Sponsor Name:The University of Oxford | |||||||||||||
Full Title: Vaccines Against Salmonella Typhi: a phase IIb, single centre, observer-blind, randomised controlled trial to assess the immunogenicity and protective efficacy of Vi conjugated (Vi-TCV) and unconju... | |||||||||||||
Medical condition: Salmonella enterica serovar Typhi infection | |||||||||||||
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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: 2020-002803-20 | Sponsor Protocol Number: APPI2-2020-AD03 | Start Date*: 2020-11-06 | |||||||||||
Sponsor Name:Parker Instituttet | |||||||||||||
Full Title: Colchicine treatment for patients with hand osteoarthritis: A randomised, placebo-controlled trial | |||||||||||||
Medical condition: Hand osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003628-18 | Sponsor Protocol Number: 000000 | Start Date*: 2020-09-29 | ||||||||||||||||
Sponsor Name:University of Oxford, Clinical Trials and Research Governance | ||||||||||||||||||
Full Title: Adalimumab in COVID-19 to present respiratory failure in community care (AVID-CC): A randomised controlled trial | ||||||||||||||||||
Medical condition: COVID-19 | ||||||||||||||||||
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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: 2021-004947-25 | Sponsor Protocol Number: NN7999-4670 | Start Date*: 2023-07-12 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A multi-centre, open-label trial evaluating efficacy, safety and pharmacokinetics of nonacog beta pegol when used for treatment and prophylaxis of bleeding episodes in Chinese patients with haemo... | |||||||||||||
Medical condition: Haemophilia B | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002267-29 | Sponsor Protocol Number: WVE-004-002 | Start Date*: 2022-10-14 | ||||||||||||||||
Sponsor Name:Wave Life Sciences UK Limited | ||||||||||||||||||
Full Title: A Multicenter, Open-label Extension (OLE) Study to Evaluate the Safety, Pharmacodynamics, and Clinical Effects of WVE-004 in Patients with C9orf72-associated Amyotrophic Lateral Sclerosis (ALS) and... | ||||||||||||||||||
Medical condition: Amyotrophic Lateral Sclerosis and Frontotemporal Dementia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) IE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001340-25 | Sponsor Protocol Number: UMC-NMZ-EPHENE2020 | Start Date*: 2020-07-17 | |||||||||||
Sponsor Name:University Medical Center Utrecht | |||||||||||||
Full Title: Enrichment randomized double-blind, placebo-controlled cross-over trial with PHEnytoin cream in patients with painful chronic idiopathic axonal polyNEuropathy | |||||||||||||
Medical condition: Painful chronic idiopathic axonal polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004822-19 | Sponsor Protocol Number: ICORG 05-11/NSABP B-38 | Start Date*: 2006-02-15 |
Sponsor Name:ICORG the all Ireland Co-operative Oncology Research Group | ||
Full Title: A Phase III, adjuvant trial comparing three chemotherapy regimens in women with node positive breast cancer: Docetaxel/Doxorubicin/Cyclophosphamide (TAC); Dose-Dense (DD) Doxorubicin/Cyclophosphami... | ||
Medical condition: Early stage node positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003238-35 | Sponsor Protocol Number: 4_141221 | Start Date*: 2021-09-15 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Effects of supplemental oxygen on systemic and cerebral hemodynamics in experimental hypovolemia: A randomized, phase IV, crossover study to study the effect of supplemental oxygen vs. room air on ... | |||||||||||||
Medical condition: Hypovolemia is the condition under investigation. Hypovolemia is induced by the "lower body negative pressure" (LBNP)-model. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003001-58 | Sponsor Protocol Number: NN7088-4595 | Start Date*: 2022-11-01 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A multi-centre, open-label trial evaluating efficacy, safety and pharmacokinetics of turoctocog alfa pegol (N8-GP) when used for treatment and prophylaxis of bleeding episodes in previously treated... | |||||||||||||
Medical condition: Haemophilia A | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002804-19 | Sponsor Protocol Number: 10975 | Start Date*: 2023-06-21 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Improving radical resection rates in patients with breast cancer by intraoperative imaging using bevacizumab-IRDye800CW – the MARGIN-2 study | ||
Medical condition: Female breast cancer patients with small tumor size in which breast conserving therapy is advised by the multidisciplinary tumor board. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-004021-71 | Sponsor Protocol Number: NL.78693.041.21 | Start Date*: 2021-10-13 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: COrticosteroids for COVID-19 induced loss of Smell – COCOS trial | ||
Medical condition: Loss of smell after COVID-19 infection, persisting after 4 weeks | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004785-33 | Sponsor Protocol Number: CMO-MA-EYE-0603 | Start Date*: 2019-05-14 | |||||||||||
Sponsor Name:Allergan Pharmaceuticals International Limited | |||||||||||||
Full Title: A 12-month, Prospective, Open-label, Phase 4 Study to Evaluate the Efficacy and Safety of OZURDEX® (Dexamethasone Intravitreal Implant) in Treatment Naïve Patients (according to standard clinical p... | |||||||||||||
Medical condition: Diabetic Macular Edema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021871-10 | Sponsor Protocol Number: IC-01-01-05-004 | Start Date*: 2012-04-18 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG - Life Science Center Innsbruck | |||||||||||||
Full Title: A multicenter, randomized, double-blinded, parallel-group, placebocontrolled study to assess the efficacy and safety of skeletal muscle-derived cell implantation in female patients with stress urin... | |||||||||||||
Medical condition: Stress urinary incontinence (SUI) of moderate severity (Grade 2 and Grade 3) in female patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) BG (Completed) AT (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000472-37 | Sponsor Protocol Number: NN1436-4479 | Start Date*: 2020-12-17 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A 26-week double blinded, multiregional, trial comparing the effect and safety of once weekly insulin icodec and once daily insulin degludec 100 units/mL, both in combination with non-insulin anti-... | |||||||||||||
Medical condition: Diabetes Mellitus, Type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) AT (Completed) DK (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000507-27 | Sponsor Protocol Number: CarbetocinHeart2014 | Start Date*: 2014-09-05 | ||||||||||||||||
Sponsor Name:Oslo University Hospital, Division of Emergencies and Critical Care | ||||||||||||||||||
Full Title: The Clinical Carbetocin Myocardium Trial | ||||||||||||||||||
Medical condition: Pregnancy | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: NO (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003163-21 | Sponsor Protocol Number: COTHUGMTRA22 | Start Date*: 2023-07-13 | |||||||||||
Sponsor Name:Coral Sánchez Pérez | |||||||||||||
Full Title: PHASE III, SINGLE-CENTER, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, LOW-INTERVENTION CLINICAL TRIAL IN TWO PARALLEL GROUPS, TO EVALUATE EFFICACY AND SAFETY IN ELDERLY PATIENTS WITH PERTROCHANTE... | |||||||||||||
Medical condition: pertrochanteric hip fracture | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000095-10 | Sponsor Protocol Number: BATCP | Start Date*: 2015-03-30 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Botulinum toxin-A as a treatment for chronic muscle-related pain in adults with spastic cerebral palsy: a randomized controlled trial. | ||
Medical condition: Spastic cerebral palsy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
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