- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    15 result(s) found for: Phlebitis.
                    
                
			
   			
		
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| EudraCT Number: 2005-005957-23 | Sponsor Protocol Number: 142/2005/U steflux | Start Date*: 2005-12-09 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
| Full Title: RANDOMIZED CLINICAL STUDY OF DIFFERENT DOSES And DURATION OF PARNAPARINA In the TREATMENT Of SUPERFICIAL VENOUS THROMBOSIS - STEFLUX STUDY | |||||||||||||
| Medical condition: superficial venous thromboses | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004774-27 | Sponsor Protocol Number: ART108053 | Start Date*: 2007-03-14 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd. | |||||||||||||
| Full Title: Comparison of ARIXTRA™ in lower LImb Superficial Thrombophlebitis with placebO (CALISTO). An International, Multicentre, Randomised, Double-blind, Placebo-controlled, Two-parallel Group, Phase III... | |||||||||||||
| Medical condition: Superficial Thrombophlebitis (also known as superficial vein thrombosis) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) NL (Completed) EE (Completed) HU (Completed) LV (Completed) GR (Completed) FR (Completed) SK (Completed) CZ (Completed) IT (Completed) GB (Completed) BG (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004880-29 | Sponsor Protocol Number: HUB-INF-RADICAP | Start Date*: 2019-10-02 | |||||||||||
| Sponsor Name:Dr. Jordi Carratalà Fernández (Servicio de Enfermedades Infecciosas) del Hospital Universitario de Bellvitge | |||||||||||||
| Full Title: Phase IV randomized, controlled, open and multicentre clinical trial with two parallel groups, to assess the impact of integral molecular tests in the antimicrobial use in community-acquired pneumo... | |||||||||||||
| Medical condition: Community-acquired pneumonia (CAP) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001559-15 | Sponsor Protocol Number: CTO#2095 | Start Date*: 2022-11-11 | |||||||||||
| Sponsor Name:Ottawa Hospital Research Institute | |||||||||||||
| Full Title: StAtins for Venous Event Reduction in Patients with Venous Thromboembolism | |||||||||||||
| Medical condition: | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-006153-31 | Sponsor Protocol Number: CSC/P01/07/Mu.F | Start Date*: 2008-04-23 | |||||||||||
| Sponsor Name:Baxter R and D Europe SCRL | |||||||||||||
| Full Title: Safety and efficacy of subcutaneous (SC) administration of Clinimix N9G15E in elderly patients at risk for malnutrition, at a dose of 1 liter infused over 12 hours for 7 to 10 consecutive days. A p... | |||||||||||||
| Medical condition: The population studied will be the elderly population at risk for malnutrition without any predefined pathology at hospital geriatrician wards. | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000284-21 | Sponsor Protocol Number: 524E-CVD-9101-004 | Start Date*: 2007-11-08 | |||||||||||
| Sponsor Name:York Hospitals NHS Foundation Trust [...] | |||||||||||||
| Full Title: A multicentre, multinational randomised control trial of prophylactic low molecular weight heparin(LMWH) in high risk pregnant thrombophilic women | |||||||||||||
| Medical condition: Thrombophilia in pregnancy. This is a multi-centre, multi-national randomised controlled trial of Low Molecular Weight Heparin to prevent pregnancy complications in high-risk pregnant thrombophi... | |||||||||||||
| 
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000755-13 | Sponsor Protocol Number: DACLEAN | Start Date*: 2020-03-31 | |||||||||||
| Sponsor Name:CHU de Poitiers | |||||||||||||
| Full Title: ESTIMATION OF THE INCIDENCE OF COLONIZATION OF PERIPHERAL VENOUS CATHETERS AFTER SKIN DISINFECTION WITH 0.5% SODIUM HYPOCHLORITE, PRECEDED OR NOT BY AN APPLICATION OF 70% ETHANOL: PILOT, MONOCENTRI... | |||||||||||||
| Medical condition: Bacterial colonization of peripheral venous catheters | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000365-33 | Sponsor Protocol Number: CHDR2043 | Start Date*: 2021-03-17 | |||||||||||
| Sponsor Name:Molecular Partners AG | |||||||||||||
| Full Title: A Phase 2a open label, non-comparative, single dose escalation study to evaluate the dynamics of viral clearance, pharmacokinetics and tolerability of ensovibep in patients with symptomatic COVID-1... | |||||||||||||
| Medical condition: SARS-CoV-2 infection (COVID-19) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004653-14 | Sponsor Protocol Number: UoL000097 | Start Date*: 2015-04-17 | 
| Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | ||
| Full Title: A Phase III, open label, multicentre randomised clinical study comparing Acelarin (NUC-1031) with Gemcitabine in patient with metastatic pancreatic carcinoma. (ACELARATE) | ||
| Medical condition: Metastatic pancreatic carcinoma. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000308-12 | Sponsor Protocol Number: P150941J | Start Date*: 2020-11-06 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS | |||||||||||||
| Full Title: « Mesenchymal stromal cells treatment in Lyell syndrome: A pilot phase 1-2 open trial” | |||||||||||||
| Medical condition: Patients: Adults diagnosed with SJS-TEN with at least 10% of body surface area involved. | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000431-32 | Sponsor Protocol Number: ORTHOUNION | Start Date*: 2017-05-25 | ||||||||||||||||
| Sponsor Name:Universidad Autónoma de Madrid (U.A.M.) | ||||||||||||||||||
| Full Title: A MULTI-CENTRE, OPEN-LABEL, RANDOMIZED, COMPARATIVE CLINICAL TRIAL OF TWO DIFFERENT DOSES OF BONE MARROW AUTOLOGOUS HUMAN MESENCHYMAL STEM CELLS PLUS BIOMATERIAL VERSUS ILIAC CREST AUTOLOGOUS GRAFT... | ||||||||||||||||||
| Medical condition: Diaphyseal and/or metaphysodiaphyseal fractures (femur, tibia, humerus) with status of non-union | ||||||||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) DE (Completed) FR (Ongoing) IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-001709-21 | Sponsor Protocol Number: 2020PI073 | Start Date*: 2020-04-29 | |||||||||||
| Sponsor Name:CHRU de Nancy | |||||||||||||
| Full Title: Effectiveness of low molecular weight heparin at increased doses prophylaxis weight-adjusted, compared with lower doses prophylaxis (intermediate or standard), on the onset of venous thromboembolis... | |||||||||||||
| Medical condition: Prevention of thromboembolic events in hospitalised COVID-19 infected patients | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014391-22 | Sponsor Protocol Number: CCBC134A2404 | Start Date*: Information not available in EudraCT | 
| Sponsor Name:Novartis Pharma AG | ||
| Full Title: An open label, multi-center, randomized, comparative Phase IIIb study to compare efficacy and safety of intravenous (i.v.) daptomycin with that of Semi-synthetic Penicillins (SSPs) or vancomycin in... | ||
| Medical condition: complicated skin and soft tissue infections. | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) IT (Completed) ES (Completed) AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-004127-21 | Sponsor Protocol Number: OP-109 | Start Date*: 2020-04-16 | |||||||||||
| Sponsor Name:Oncopeptides AB | |||||||||||||
| Full Title: A randomized, two-period, cross-over, Phase 2 study, comparing the pharmacokinetics, and assessing safety and tolerability of peripheral and central intravenous administration of melflufen in patie... | |||||||||||||
| Medical condition: Patients with relapsed and refractory multiple myeloma. | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) BG (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001024-34 | Sponsor Protocol Number: OraPAT-IE-GAMES | Start Date*: 2021-12-15 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Oral antimicrobial treatment vs. outpatient parenteral for infective endocarditis. | |||||||||||||
| Medical condition: infective endocarditis | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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