- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Laser coagulation.
Displaying page 1 of 1.
EudraCT Number: 2005-003288-21 | Sponsor Protocol Number: EURIVAT2 | Start Date*: 2005-09-28 |
Sponsor Name:Dept. of Ophthalmology, Medical University of Vienna | ||
Full Title: INTRAOCULAR BEVACIZUMAB (AVASTIN™) FOR CENTRAL AND BRANCH RETINAL VEIN OCCLUSION STUDY | ||
Medical condition: CENTRAL AND BRANCH RETINAL VEIN OCCLUSION | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-005197-23 | Sponsor Protocol Number: 1/1 | Start Date*: 2005-10-06 |
Sponsor Name:Klinik und Poliklinik für Augenheilkunde der Universität Regensburg | ||
Full Title: Funktionelle Ergebnisse der intravitrealen Injektion von Triamcinolonacetonid im Vergleich zur konventionellen Lasertherapie bei diabetischem Makulaödem. | ||
Medical condition: Patients with diffuse macular edema due to diabetic retinopathy and decrease in visual acuity. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001553-26 | Sponsor Protocol Number: Protocol 03_10_2007 | Start Date*: 2008-03-13 | |||||||||||
Sponsor Name:Vienna Medical University, Dept. of Ophthalmology | |||||||||||||
Full Title: A randomized, double-masked study with intraocular bevacizumab (Avastin®) compared with intraocular triamcinolone (Volon A®) in patients with clinical significant diabetic macular edema | |||||||||||||
Medical condition: Patients with persisting macular edema due to diabetic retinopathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020902-13 | Sponsor Protocol Number: 0001-2010 | Start Date*: 2011-07-22 |
Sponsor Name:Universitätsklinik für Augenheilkunde und Optometrie, Medizinische Universität Innsbruck | ||
Full Title: Intravitreal Lucentis (Ranibizumab) in acute central serous Chrioretinopathy - a prospective, randomized, single blind monocentric study | ||
Medical condition: Acute central serous chorioretinopathy (CSC) CSC is an acute idiopathic chorioretinopathy. While the majority of cases is characterized by a self-limited course, chronic CSC is seen in up to one t... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-003491-23 | Sponsor Protocol Number: 4C-2014-06 | Start Date*: 2014-10-10 |
Sponsor Name:AIBILI – Association for Innovation and Biomedical Research on Light and Image | ||
Full Title: A non-randomised, open-label, multicenter phase 4 pilot study on the effect and safety of Iluvien® in chronic diabetic macular edema patients considered insufficiently responsive to available thera... | ||
Medical condition: Chronic Diabetic Medical Edema | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001469-28 | Sponsor Protocol Number: SA2008 | Start Date*: 2009-06-17 | |||||||||||
Sponsor Name:Dep. of Ophthalmology, Medical University of Vienna | |||||||||||||
Full Title: A randomized, double-masked study with intraocular Bevacizumab (Avastin®) compared with intravitreal Ranibizumab (Lucentis®) in patients with persistent diabetic macular edema or persistent active ... | |||||||||||||
Medical condition: persistent diabetic macula edema or persistent diabetic proliferative retinopathy after lasercoagulation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013157-15 | Sponsor Protocol Number: 1218.74 | Start Date*: 2010-10-14 | |||||||||||
Sponsor Name:SCS Boehringer Ingelheim Comm.V | |||||||||||||
Full Title: A multicentre, international, randomised, parallel group, double blind study to evaluate Cardiovascular safety of linagliptin versus glimepiride in patients with type 2 diabetes mellitus at high ca... | |||||||||||||
Medical condition: Patients with documented diagnosis of T2DM with insufficient glycaemic control and at high risk of CV events prior to informed consent can be enrolled in the study. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) DE (Completed) PT (Completed) CZ (Completed) ES (Completed) IE (Completed) FI (Completed) SE (Completed) GB (Completed) SK (Completed) IT (Completed) GR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001312-59 | Sponsor Protocol Number: CRO1824 | Start Date*: 2011-06-24 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A double-blinded, randomized, crossover clinical study to assess the efficacy of Qutenza (capsaicin 8% patches) for the reduction of site pain caused by continuous subcutaneous infusion of Remoduli... | |||||||||||||
Medical condition: Pulmonary arterial hypertension (PAH) is a rare life-threatening disease characterised by high blood pressure in the arteries to the lungs, rapidly evolving in a clinical syndrome of dyspnoea and f... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003326-41 | Sponsor Protocol Number: 200719 | Start Date*: 2016-01-13 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: Randomized, Double-Blind, Multicenter, Phase III Study Comparing the Efficacy and Safety of Retosiban Versus Placebo for Women in Spontaneous Preterm Labor | |||||||||||||
Medical condition: Preterm Labour | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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