- Trials with a EudraCT protocol (171)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
171 result(s) found for: Neovascularization.
Displaying page 1 of 9.
EudraCT Number: 2007-003253-88 | Sponsor Protocol Number: 802/07 | Start Date*: 2008-04-04 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: morpho-functional evaluation of eye disease with corneal neovascularitation after subconjuctival injection of bevacizumab. Interventional pilot study. | |||||||||||||
Medical condition: disease with corneal neovascularization | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005945-39 | Sponsor Protocol Number: HLS03/2007 | Start Date*: 2008-01-30 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Phase II open label study of Pegaptanib sodium on patients with subfoveal choroidal neovascularization caused by pathologic myopia. | |||||||||||||
Medical condition: Patients with choroidal neovascularization secondary to pathologic myopia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002424-42 | Sponsor Protocol Number: 2006-002 | Start Date*: 2006-03-20 | |||||||||||
Sponsor Name:OSPEDALE SACRO CUORE-DON CALABRIA | |||||||||||||
Full Title: Evaluation of Safety and Efficacy on Visual Acuity Outcome and Choroidal Neovascularization of Intravitreal Somministration of Bevacizumab Avastin, Roche, United Kingdom in patients with Subfovea... | |||||||||||||
Medical condition: Subfoveal Choroidal Neovascularization due to Age Related Macular Degeneration who did not respond to currently available treatments | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001781-15 | Sponsor Protocol Number: IOBA-04-2012 | Start Date*: 2012-07-31 | |||||||||||
Sponsor Name:IOBA, Universidad de Valladolid | |||||||||||||
Full Title: Initial protocol setting for the treatment of choroidal neovascularization associated to myopia magna with intravitreal bevacizumab: 3 vs 1 (BENEMCOR.es study) | |||||||||||||
Medical condition: choroidal neovascularization associated to myopia magna | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007787-25 | Sponsor Protocol Number: RE OC-02/2007 | Start Date*: 2007-12-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE S. MARIA NUOVA | |||||||||||||
Full Title: Use of subconjunctival Bevacizumab (Avastin) in treatment of corneal neovascularization non curable with standard protocols (topical and sistemic steroids). | |||||||||||||
Medical condition: Corneal neovascularization | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022858-16 | Sponsor Protocol Number: I07034 | Start Date*: 2011-06-27 | |||||||||||
Sponsor Name:CHU de Limoges | |||||||||||||
Full Title: EFFECT OF BEVACIZUMAB SUBCONJUNCTIVAL INJECTIONS ON CORNEAL NEWVESSELS | |||||||||||||
Medical condition: Corneal neovascularisation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001640-38 | Sponsor Protocol Number: ATTRACT | Start Date*: 2014-08-08 | |||||||||||
Sponsor Name:CHU DE POITIERS | |||||||||||||
Full Title: Efficacy of Aflibercept (Eylea®) on Type 3 choroidal neovascularization. | |||||||||||||
Medical condition: Retinal diseases (type 3 choroidal neovascularization) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007984-17 | Sponsor Protocol Number: PETC1002 | Start Date*: 2009-03-02 | |||||||||||
Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | |||||||||||||
Full Title: Pilot randomised placebo-controlled double-masked clinical trial of subconjunctival Bevacizumab on eyes with recent onset of corneal neovascularisation | |||||||||||||
Medical condition: Corneal neovascularisation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017161-28 | Sponsor Protocol Number: EO031109 | Start Date*: 2010-01-19 | |||||||||||
Sponsor Name:Juha Holopainen | |||||||||||||
Full Title: VEGF-estäjä bevasitsumabi sarveiskalvon uudissuonituksen hoidossa. | |||||||||||||
Medical condition: Tutkittavilla henkilöillä on sarveiskalvolla patologinen uudissuonitus, jonka etiologia voi olla esim. keratiitti tai limbusalueen sairaus. Sarveiskalvon uudissuonitus johtaa sarveiskalvon samentum... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020683-38 | Sponsor Protocol Number: CHUBX 2009/30 | Start Date*: 2010-07-23 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Injection sous-conjonctivale de ranibizumab (Lucentis®) dans le traitement de la néovascularisation cornéenne : étude pilote de phase I/II | |||||||||||||
Medical condition: néovascularisation cornéenne | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000986-30 | Sponsor Protocol Number: 140109 | Start Date*: 2015-03-03 | |||||||||||
Sponsor Name:IRCCS Ospedale San Raffaele U.O. Oculistica | |||||||||||||
Full Title: Intravitreal Aflibercept for Choroidal Neovascularization Secondary to Angioid Streaks (EYLEA-STRIE) | |||||||||||||
Medical condition: Choroidal neovascularization secondary to angioid streaks . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001453-28 | Sponsor Protocol Number: CRFB002B2201 | Start Date*: 2004-11-19 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: Open-label, Multicenter, Phase II Study Assessing the Safety of Lucentis (ranibizumab) Administered in Conjunction with Photodynamic Therapy with Visudyne in Patients with Occult or Predominantly C... | |||||||||||||
Medical condition: Male and female patients > 50 years of age with subfoveal choroidal neovascularization (CNV) secondary to AMD. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006235-31 | Sponsor Protocol Number: RET 03.07 | Start Date*: 2007-09-13 | |||||||||||
Sponsor Name:IRCCS- FONDAZIONE G.B. BIETTI PER LO STUDIO E LA RICERCA IN OFTALMOLOGIA-ONLUS | |||||||||||||
Full Title: 12 MONTHS CASE SERIES OPEN STUDY TO ASSESS THE SAFETY AND EFFICACY OF INTRAVITREAL INJECTION OF LUCENTIS (RANIBIZUMAB 0.5 MG) USED IN COMBINATION WITH VISUDYNE (VERTEPORFIN PDT) IN NAIVE SIBJECTS W... | |||||||||||||
Medical condition: subfoveal choroidal neovascularization secondary to age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014854-14 | Sponsor Protocol Number: CRFB002AGB10 | Start Date*: 2009-11-17 | ||||||||||||||||
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||||||||||||||||||
Full Title: A phase II, open-label, multicentre, 12 month study to evaluate the efficacy and safety of ranibizumab (0.5 mg) in patients with choroidal neovascularization secondary to pathological myopia (PM) | ||||||||||||||||||
Medical condition: Choroidal neovascularisation (CNV) secondary to pathological myopia (PM) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022473-33 | Sponsor Protocol Number: Protocol 21_07_2010 | Start Date*: 2010-10-06 | |||||||||||
Sponsor Name:Department of Ophthalmology, Hietzing Hospital | |||||||||||||
Full Title: Short term effect of Lucentis® (Ranibizumab) as pretreatment to laser photocoagulation versus Lucentis® (Ranibizumab) combined with laser photocoagulation in the treatment of diabetic macular edema... | |||||||||||||
Medical condition: Patients with macular edema due to diabetic retinopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005081-19 | Sponsor Protocol Number: 1 | Start Date*: 2014-07-10 | |||||||||||
Sponsor Name:HOSPICES CIVILS DELYON | |||||||||||||
Full Title: Phase II study evaluating the efficacy of aflibercept for the treatment of idiopathic choroidal neovascularization in young subjects: the INTUITION study | |||||||||||||
Medical condition: idiopathic choroidal neovascularization | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014612-34 | Sponsor Protocol Number: CRFB002APT02T | Start Date*: 2011-09-12 | |||||||||||
Sponsor Name:AIBILI - Association for Innovation and Biomedical Research on Light and Image | |||||||||||||
Full Title: Prospective, multicenter, open-label study to evaluate the safety and efficacy of intravitreal ranibizumab in patients with subfoveal or juxtafoveal choroidal neovascularization (CNV) secondary to ... | |||||||||||||
Medical condition: Patients with subfoveal or juxtafoveal choroidal neovascularization secondary to other causes than Age-related Macular Degeneration and Pathological Myopia (angioid streaks, pseudohistoplasmosis, i... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004172-12 | Sponsor Protocol Number: CBPD952A2309 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 24-month randomized, double-masked, multicenter, phase II study assessing safety and efficacy of verteporfin (Visudyne®) photodynamic therapy administered in conjunction with Lucentis™ versus Luc... | |||||||||||||
Medical condition: Subfoveal choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) AT (Prematurely Ended) IT (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) DK (Prematurely Ended) FR (Prematurely Ended) BE (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005056-15 | Sponsor Protocol Number: AGO/2013/012 | Start Date*: 2014-03-21 | ||||||||||||||||
Sponsor Name:UZ Gent | ||||||||||||||||||
Full Title: Longterm efficiency and safety of intravitreal injections with bevacizumab in patients with neovascularisation or macular edema. | ||||||||||||||||||
Medical condition: Choroidal neovascularisation and chronic macular edema | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-003334-33 | Sponsor Protocol Number: CRFB002FIT01 | Start Date*: 2013-12-16 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A 12-month, open-label, interventional, multicentre study to investigate the current criteria driving re-treatment with ranibizumab upon relapse in patients with visual impairment due to choroidal ... | |||||||||||||
Medical condition: Choroidal neovascularization secondary to pathologic myopia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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