- Trials with a EudraCT protocol (1,302)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,302 result(s) found for: Vascular diseases.
Displaying page 3 of 66.
EudraCT Number: 2006-006191-38 | Sponsor Protocol Number: 004SC06084 | Start Date*: 2007-01-11 | |||||||||||
Sponsor Name:ANGELINI | |||||||||||||
Full Title: The effects of the association bindarit irbesartan versus irbesartan alone on albuminuria of patients with Diabetic Nephropathy. Placebo-controlled study. | |||||||||||||
Medical condition: Patients with type II diabetes with nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003674-32 | Sponsor Protocol Number: 1.1:12-6-2015 | Start Date*: 2016-02-23 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of Telmisartan on inflammatory processes in the vascular wall of abdominal aortic aneurysms. | ||
Medical condition: Abdominal aortic aneurysm with an indication for elective open surgical repair. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000123-33 | Sponsor Protocol Number: RH EPOA-REHAB | Start Date*: 2011-06-01 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust [...] | |||||||||||||
Full Title: Evaluation of the feasibility of modulating and measuring endogenous neurogenesis with erythropoietin (rhEPOα) to expedite recovery after stroke | |||||||||||||
Medical condition: Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021437-30 | Sponsor Protocol Number: PAISII-V01 | Start Date*: 2011-02-04 | |||||||||||
Sponsor Name:ErasmusMC | |||||||||||||
Full Title: Paracetamol (Acetaminophen) in Stroke 2 (PAIS 2): A randomized, placebo-controlled clinical trial of high-dose paracetamol in patients with acute stroke and a body temperature of 36.5°C or above | |||||||||||||
Medical condition: acute stroke (cerebral infarction or intracrebral hemorrhage) and a body temperature of 36.5 degrees or above. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005401-20 | Sponsor Protocol Number: CSLCT-BIO-03-97 | Start Date*: 2015-01-30 | |||||||||||
Sponsor Name:CSL Limited | |||||||||||||
Full Title: An Open-label, Multi-centre Study to Assess the Efficacy and Safety of Biostate® in Patients With von Willebrand's Disease (VWD) | |||||||||||||
Medical condition: Von Willebrand's disease (VWD) | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000044-34 | Sponsor Protocol Number: BT200-VWD2B | Start Date*: 2024-08-14 | |||||||||||
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | |||||||||||||
Full Title: Efficacy and Safety of BT200 (rondoraptivon pegol) in Patients with Type 2B von Willebrand disease | |||||||||||||
Medical condition: patients with type 2B Von Willebrand Disease with thrombocytopenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001910-25 | Sponsor Protocol Number: WIL-21 | Start Date*: 2008-07-17 | |||||||||||
Sponsor Name:Octapharma AG | |||||||||||||
Full Title: Pharmacokinetics of WILATE® and Haemate® P in von Willebrand type 3 patients - a prospective, randomised, controlled, open-labelled, 2-arm cross-over study | |||||||||||||
Medical condition: Inherited von Willebrand Disease (VWD) type 3 | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005051-34 | Sponsor Protocol Number: 42-73-305 / WIL1-0305 | Start Date*: 2005-04-18 | |||||||||||
Sponsor Name:LFB BIOTECHNOLOGIES | |||||||||||||
Full Title: Efficacy and safety study of vWF SD-35-DH (WILFACTIN) in children under 6 years of age | |||||||||||||
Medical condition: Von Willebrand disease | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004980-63 | Sponsor Protocol Number: 191622-116 | Start Date*: 2012-02-08 | ||||||||||||||||
Sponsor Name:Allergan Ltd. | ||||||||||||||||||
Full Title: BOTOX® Treatment in Adult Patients with Post-Stroke Lower Limb Spasticity | ||||||||||||||||||
Medical condition: Post-Stroke Lower Limb Spasticity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) DE (Completed) GB (Completed) CZ (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001096-43 | Sponsor Protocol Number: PHRN14-AM/PERFORMUS | Start Date*: 2015-07-10 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Treatment of superficial voluminous complicated slow-flow vascular malformations with sirolimus: a phase 2 trial in children observational-phase designed | |||||||||||||
Medical condition: vascular malformations | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024108-84 | Sponsor Protocol Number: 071001 | Start Date*: 2011-10-31 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: A PHASE 3 CLINICAL STUDY TO DETERMINE THE PHARMACOKINETICS, SAFETY AND EFFICACY OF rVWF:rFVIII and rVWF IN THE TREATMENT OF BLEEDING EPISODES IN SUBJECTS DIAGNOSED WITH VON WILLEBRAND DISEASE | |||||||||||||
Medical condition: Von Willebrand Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) SE (Completed) AT (Completed) NL (Completed) BE (Completed) BG (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003949-41 | Sponsor Protocol Number: 36810 | Start Date*: 2014-11-06 |
Sponsor Name:VU medical Center | ||
Full Title: Role of different phosphate binders on absorption of vitamin K, metabolism of matrix γ-carboxy-glutamaat (Gla) proteïne (MGP). | ||
Medical condition: Vascular calcification, phosphate binders and patients on hemodialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001888-39 | Sponsor Protocol Number: PGX-HT | Start Date*: 2016-01-28 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: PHARMACOGENOMICS HYPERTENSION : A NEW APPROACH FOR PERSONALIZED MEDICINE ( PGX - HT ) | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000022-75 | Sponsor Protocol Number: CV131-169 | Start Date*: 2004-09-24 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: Irbesartan Versus Placebo in Combination with Standard Cardiovascular Protection ACE-I Therapy with Ramipril for the Treatment of Albuminuria in Hypertensive Subjects at Elevated Cardiovascular Risk | ||
Medical condition: Albuminuria in hypertensive subjects at increased cardiovascular risk. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LT (Completed) LV (Completed) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002935-27 | Sponsor Protocol Number: 41208 | Start Date*: 2012-12-13 | |||||||||||||||||||||||||||||||
Sponsor Name:Maastricht University Medical Center | |||||||||||||||||||||||||||||||||
Full Title: Diagnostic value of novel MR imaging techniques for the primary staging and restaging of rectal cancer | |||||||||||||||||||||||||||||||||
Medical condition: rectal cancer | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018421-19 | Sponsor Protocol Number: PASS | Start Date*: 2010-05-05 | ||||||||||||||||
Sponsor Name:AMC | ||||||||||||||||||
Full Title: Preventive Antibiotics in Stroke Study | ||||||||||||||||||
Medical condition: Stroke and stroke-associated infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003305-25 | Sponsor Protocol Number: CSLCT-BIO-12-83 | Start Date*: 2015-07-07 | |||||||||||
Sponsor Name:CSL Behring GmbH | |||||||||||||
Full Title: An Open-label, Multi-centre Post-marketing Study to Assess the Efficacy and Safety of Voncento® in Subjects with Von Willebrand Disease | |||||||||||||
Medical condition: Von Willebrand Disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) AT (Completed) IE (Completed) PL (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004494-23 | Sponsor Protocol Number: MAG104615 | Start Date*: 2013-03-18 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: Study MAG104615, a Proof of Concept Study for GSK249320 versus placebo in Stroke Patients | |||||||||||||
Medical condition: Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000103-27 | Sponsor Protocol Number: Eylea-2014 | Start Date*: 2014-03-12 |
Sponsor Name: | ||
Full Title: Plasma levels of vascular endothelial growth factor before and after intravitreal injection of aflibercept in patients with exudative age-related macular degeneration. | ||
Medical condition: Exudative age-related macular degeneration (AMD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002346-37 | Sponsor Protocol Number: 191622-127 | Start Date*: 2014-05-21 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: BOTOX® Treatment in Adult Patients with Upper Limb Spasticity | |||||||||||||||||||||||
Medical condition: Poststroke spasticity involving the muscles of the elbow and shoulder in adult patients | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
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