- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
49 result(s) found for: Central retinal vein.
Displaying page 2 of 3.
EudraCT Number: 2016-004648-12 | Sponsor Protocol Number: CLS1003-301 | Start Date*: 2018-01-15 |
Sponsor Name:Clearside Biomedical, Inc. | ||
Full Title: SAPPHIRE: A RANDOMIZED, MASKED, CONTROLLED TRIAL TO STUDY THE SAFETY AND EFFICACY OF SUPRACHOROIDAL CLS-TA IN CONJUNCTION WITH INTRAVITREAL AFLIBERCEPT IN SUBJECTS WITH RETINAL VEIN OCCLUSION | ||
Medical condition: Retinal Vein Occlusion | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) HU (Completed) DE (Prematurely Ended) ES (Prematurely Ended) AT (Prematurely Ended) PT (Completed) DK (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-001842-33 | Sponsor Protocol Number: CRTH258C2301 | Start Date*: 2019-06-14 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: An Eighteen-Month, Two-Arm, Randomized, Double Masked, Multi center, Phase III Study Assessing the Efficacy and Safety of Brolucizumab versus Aflibercept in Adult Patients with Visual Impairment du... | |||||||||||||
Medical condition: Branch retinal vein occlusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) DK (Prematurely Ended) ES (Prematurely Ended) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001047-21 | Sponsor Protocol Number: 690110 | Start Date*: 2014-06-09 |
Sponsor Name:Sankt Eriks Eye Hospital | ||
Full Title: Randomized trial comparing injection frequency between Aflibercept and Ranibizumab in patients with Central Retinal Vein Occlusion with a treat and extent algorithm | ||
Medical condition: Central retinal vein occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005045-13 | Sponsor Protocol Number: CRFB002EDE20 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: An open-label, multi-center, 6-month extension study comparing the long-term efficacy and safety of Lucentis (Ranibizumab) intravitreal injections versus Ozurdex (Dexamethasone) intravitreal implan... | |||||||||||||
Medical condition: visual impairment due to macular edema following retinal vein occlusion (branch or central) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001727-19 | Sponsor Protocol Number: 45/2006/U/Sper | Start Date*: 2006-10-03 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Triamcinolone Acetonide Intravitreal Injection for the treatment for exudative maculopathy | |||||||||||||
Medical condition: exudative maculopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005468-25 | Sponsor Protocol Number: CRFB002ANO01 | Start Date*: 2007-01-24 | |||||||||||
Sponsor Name:Retinaklinikken Aleris | |||||||||||||
Full Title: A randomized study comparing the safety and efficacy of ranibizumab (Lucentis ®) to sham in patients with macular edema secondary to central retinal vein occlusion (CRVO). | |||||||||||||
Medical condition: Macular edema secondary to central retinal vein occlusion (CRVO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005449-18 | Sponsor Protocol Number: MMT_2020_33 | Start Date*: 2021-03-08 |
Sponsor Name:Hôpital Fondation A. de Rothschild / Service de recherche clinique | ||
Full Title: Spontaneous retinal artery pulses as a prognostic determinant of central retinal vein occlusions in patients with and without intravitreal aflibercept injections. | ||
Medical condition: Central retinal vein occlusions | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001678-25 | Sponsor Protocol Number: 138/06 | Start Date*: 2006-02-16 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Macular structure and function after intravitreal injection of bevacizumab for vascular retinopathy a interventional study. | |||||||||||||
Medical condition: vascular retinopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000975-21 | Sponsor Protocol Number: RET-AFLI-2014-01 | Start Date*: 2014-06-16 |
Sponsor Name:Fundación Retinaplus + | ||
Full Title: A phase IV study to evaluate the effectiveness of aflibercept in naive patients with macular edema secondary to Central Retinal Vein Occlusion (CRVO) on an individualized Treat and Extend regimen. ... | ||
Medical condition: Macular edema secondary to central retinal vein occlusion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
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: 2011-002350-31 | Sponsor Protocol Number: CRFB002E2401 | Start Date*: 2012-02-24 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A 24-month, phase IIIb, open-label, single arm, multicenter study assessing the efficacy and safety of an individualized, stabilization criteria-driven PRN dosing regimen with 0.5-mg ranibizumab in... | |||||||||||||||||||||||
Medical condition: visual impairment due to macular edema secondary to central retinal vein occlusion (CRVO) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) IE (Completed) SE (Completed) HU (Completed) AT (Completed) ES (Completed) CZ (Completed) SK (Completed) GR (Completed) PT (Completed) NL (Completed) PL (Completed) IT (Completed) DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002826-31 | Sponsor Protocol Number: V1 | Start Date*: 2007-11-09 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Response of retinal vessels to anti vascular endothelial growth factor (VEGF) treatment in patients with branch retinal vein occlusion (BRVO) | ||
Medical condition: Cystoid macular oedema due to branch retinal vein occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001020-38 | Sponsor Protocol Number: CRFB002EDE18 | Start Date*: 2011-06-24 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 6-month multicenter, randomized, double-masked phase IIIb-study comparing the efficacy and safety of Lucentis (Ranibizumab) intravitreal injections versus Ozurdex (Dexamethasone) intravitreal imp... | |||||||||||||
Medical condition: visual impairment due to macular edema following central retinal vein occlusion (CRVO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001143-12 | Sponsor Protocol Number: 11-EI-0264 | Start Date*: 2018-01-09 |
Sponsor Name:The National Eye Institute | ||
Full Title: A Pilot Study for the Evaluation of Minocycline as a Microglia Inhibitor in the Treatment of Central Retinal Vein Occlusions | ||
Medical condition: Central Retinal Vein Occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006131-53 | Sponsor Protocol Number: AU-06104G | Start Date*: 2007-08-02 | |||||||||||
Sponsor Name:Society (institute) for clinical research | |||||||||||||
Full Title: Ranibizumab for Branch Retinal Vein Occlusion Associated Macular Edema Study | |||||||||||||
Medical condition: Macular edema secondary to branch retinal vein occlusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001179-21 | Sponsor Protocol Number: 11-EI-0263 | Start Date*: 2018-01-17 |
Sponsor Name:The National Eye Institute | ||
Full Title: A Pilot Study for the Evaluation of Minocycline as a Microglia Inhibitor in the Treatment of Branch Retinal Vein Occlusions | ||
Medical condition: Branch Retinal Vein Occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006265-93 | Sponsor Protocol Number: AVO1 | Start Date*: 2009-03-11 |
Sponsor Name:St Eriks Eye Hospital | ||
Full Title: A prospective, randomized, masked and controlled trial of intravitreal bevacizumab (Avastin®) for central retinal vein occlusion (CRVO). | ||
Medical condition: Central retinal vein occlusion (CRVO) is a sight-threatening ocular condition without efficient treatment. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023110-30 | Sponsor Protocol Number: Octome | Start Date*: 2011-04-11 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: An exploratory phase III prospective open-label clinical study on monthly OCT monitoring of the effects of Ozurdex for macular oedema related to retinal vascular diseases | |||||||||||||
Medical condition: Macular oedema related to retinal vascular diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001019-30 | Sponsor Protocol Number: CRFB002EDE17 | Start Date*: 2011-06-01 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 6-month multicenter, randomized, double-masked phase IIIb-study comparing the efficacy and safety of Lucentis (Ranibizumab) intravitreal injections versus Ozurdex (Dexamethasone) intravitreal imp... | |||||||||||||
Medical condition: visual impairment due to macular edema following branch retinal vein occlusion (BRVO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002089-37 | Sponsor Protocol Number: CLS1003-302 | Start Date*: 2018-09-27 |
Sponsor Name:Clearside Biomedical, Inc. | ||
Full Title: TOPAZ: A RANDOMIZED, MASKED, CONTROLLED TRIAL TO STUDY THE SAFETY AND EFFICACY OF SUPRACHOROIDAL CLS-TA IN COMBINATION WITH AN INTRAVITREAL ANTI-VEGF AGENT IN SUBJECTS WITH RETINAL VEIN OCCLUSION | ||
Medical condition: Retinal Vein Occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) HU (Completed) EE (Prematurely Ended) | ||
Trial results: View results |
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