- Trials with a EudraCT protocol (22)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
22 result(s) found for: Vitreous Hemorrhage.
Displaying page 1 of 2.
EudraCT Number: 2009-015559-25 | Sponsor Protocol Number: KCH1724 | Start Date*: 2010-04-22 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: Preoperative intravitreal ranibizumab for persistent diabetic vitreous haemorrhage: A randomized, double-masked, controlled study | |||||||||||||
Medical condition: Retinopathy is a well recognised complication of diabetes and is a leading cause of vision loss in this patient group. The severity of diabetic retinopathy varies, but in its most severe form (pro... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003297-81 | Sponsor Protocol Number: PDRPOZU1 | Start Date*: 2011-09-12 | |||||||||||
Sponsor Name:St Eriks Eye Hospital | |||||||||||||
Full Title: A prospective, randomized study on intravitreal Ozurdex for preventing recurrent vitreous hemorrhage following pars plana vitrectomy for proliferative diabetic retinopathy | |||||||||||||
Medical condition: Proliferative diabetic retinopathy | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018919-16 | Sponsor Protocol Number: TG-MV-010 | Start Date*: 2010-06-28 | |||||||||||
Sponsor Name:ThromboGenics NV | |||||||||||||
Full Title: An Open-Label, Ascending- Exposure-Time, Single Center Trial to Evaluate the Pharmacokinetic Properties of Ocriplasmin (Generic Name of the Molecule Microplasmin) Intravitreal Injection in Subjects... | |||||||||||||
Medical condition: Patients who require primary pars plana vitrectomy. A sample of vitreous will be taken at beginning of surgery for PK analysis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001421-55 | Sponsor Protocol Number: CRFB002GFR02 | Start Date*: 2013-06-13 | |||||||||||
Sponsor Name:Novartis Pharma S.A.S | |||||||||||||
Full Title: An open-label Extended Clinical Protocol of ranibizumab to evaluate Safety and Efficacy in rare VEGF driven ocular diseases. | |||||||||||||
Medical condition: Choroidal neovascularization not related to wet Age-related macular degeneration (wAMD), pathologic myopia (PM)or Pseudoxanthoma elasticum (PXE), as well as in Macular Edema (ME) not related to Ret... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018637-21 | Sponsor Protocol Number: 1 | Start Date*: 2013-11-20 | ||||||||||||||||
Sponsor Name:Universitätsklinikum Schleswig-Holstein UKSH | ||||||||||||||||||
Full Title: Intravitreal Injection of Lucentis (Ranibizumab) after Pars Plana Vitrectomy and Subretinal Application of Recombinant Tissue Plasminogen Activator (rtPA) in Patients with Acute Submacular Hemorrha... | ||||||||||||||||||
Medical condition: exsudative age-related macular degeneration with acut submacular hemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006085-42 | Sponsor Protocol Number: TG-MV-004 | Start Date*: 2007-01-24 | |||||||||||
Sponsor Name:ThromboGenics Ltd. | |||||||||||||
Full Title: A Randomized, Sham-Injection Controlled, Double-Masked, Ascending-Dose, Dose-Range-Finding, Multicenter Trial of Microplasmin Intravitreal Injection for Non-Surgical PVD Induction for Treatment of ... | |||||||||||||
Medical condition: Vitreomacular Traction Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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: 2018-000753-45 | Sponsor Protocol Number: NAVIT-18 | Start Date*: 2018-11-11 |
Sponsor Name:NAVARRBIOMED-FUNDACION MIGUEL SERVET | ||
Full Title: Vitreretinal surgery with and without oral anticoagulants: surgical complications, visual results and perioperative thromboembolic events. | ||
Medical condition: Patients undergoing vitreoretinal surgery under treatment with oral anticoagulants | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003640-23 | Sponsor Protocol Number: ECR-RET-2013-05 | Start Date*: 2014-01-13 | |||||||||||
Sponsor Name:AIBILI - Association for Innovation and Biomedical Research on Light and Image | |||||||||||||
Full Title: Prospective, randomized, multicentre, open label, phase II / III study to assess efficacy and safety of ranibizumab 0.5 mg intravitreal injections plus panretinal photocoagulation (PRP) versus PRP ... | |||||||||||||
Medical condition: Patients with type I or type II diabetes mellitus and high risk diabetic retinopathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004626-93 | Sponsor Protocol Number: TG-MV-002 | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:ThromboGenics N.V. | |||||||||||||
Full Title: A Randomized, Sham-Injection Controlled, Double-Masked, Ascending-Dose, Dose-Range-Finding Trial of Microplasmin Intravitreal Injection for Non-Surgical PVD Induction for Treatment of Diabetic Macu... | |||||||||||||
Medical condition: Diabetic macular edema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) NL (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005228-10 | Sponsor Protocol Number: TG-MV-008 | Start Date*: 2008-10-03 | |||||||||||
Sponsor Name:ThromboGenics NV | |||||||||||||
Full Title: An Open Label, Single Center Trial of Microplasmin Intravitreal Injection for Non-Surgical Treatment of Focal Vitreomacular Adhesion | |||||||||||||
Medical condition: Focal vitreomacular adhesion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001171-36 | Sponsor Protocol Number: TG-MV-001 | Start Date*: 2005-05-13 |
Sponsor Name:ThromboGenics Ltd. | ||
Full Title: A Dose-Escalation Clinical Trial of Intravitreal Microplasmin in Patients Undergoing Surgical Vitrectomy for Vitreomacular Traction Maculopathy | ||
Medical condition: Vitreomacular Traction Maculopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005601-22 | Sponsor Protocol Number: poc1doxy | Start Date*: 2008-03-27 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Proof–of–concept study 1 (POC1): Evaluation of effect of doxycycline versus placebo on retinal function and posterior segment neovascularization in patients with severe non-proliferative or early ... | |||||||||||||
Medical condition: Diabetic retinopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014409-15 | Sponsor Protocol Number: CRFB002DPT04T | Start Date*: 2010-01-08 | |||||||||||
Sponsor Name:AIBILI - Association for Innovation and Biomedical Research on Light and Image | |||||||||||||
Full Title: Prospective, randomized, multicenter, open label phase II study to access efficacy and safety of Lucentis monotherapy (ranibizumab 0.5 mg intravitreal injections) compared with Lucentis plus panret... | |||||||||||||
Medical condition: Proliferative Diabetic Retinopathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016760-36 | Sponsor Protocol Number: CC-02-2009 | Start Date*: 2010-02-05 | |||||||||||
Sponsor Name:AIBILI | |||||||||||||
Full Title: Prospective, randomized, open label phase II study to assess efficacy and safety of Macugen® (pegaptanib 0.3 mg intravitreal injections) plus panretinal photocoagulation (PRP) and PRP (monotherapy)... | |||||||||||||
Medical condition: Proliferative Diabetic Retinopathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003243-37 | Sponsor Protocol Number: | Start Date*: 2017-11-02 | |||||||||||||||||||||||||||||||
Sponsor Name:MUST Coordinating Centre, John Hopkins Bloomberg School of Public Health | |||||||||||||||||||||||||||||||||
Full Title: Macular Edema Ranibizumab v. Intravitreal anti-inflammatory Therapy (MERIT) Trial | |||||||||||||||||||||||||||||||||
Medical condition: Uveitic macular oedema | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Temporarily Halted) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000304-29 | Sponsor Protocol Number: | Start Date*: 2016-04-05 | |||||||||||||||||||||||||||||||
Sponsor Name:MUST Coordinating Centre, John Hopkins Bloomberg School of Public Health | |||||||||||||||||||||||||||||||||
Full Title: Periocular and Intravitreal Corticosteroids for Uveitic Macular Edema (POINT) Trial | |||||||||||||||||||||||||||||||||
Medical condition: Uveitic macular oedema | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000642-35 | Sponsor Protocol Number: HL217-201 | Start Date*: 2019-09-19 | |||||||||||
Sponsor Name:HANLIM PHARM CO., LTD | |||||||||||||
Full Title: A phase IIa randomized, double-blind, multicentre study to evaluate safety and efficacy of HL217 topical ophthalmologic solution in the treatment of exudative Age-Related Macular Degeneration (AMD) | |||||||||||||
Medical condition: AMD (age-related macular degeneration) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003165-13 | Sponsor Protocol Number: 03 | Start Date*: 2007-02-15 | |||||||||||
Sponsor Name:Dep. Ophthalmology, Medical University of Vienna | |||||||||||||
Full Title: A randomized, double-masked study with intraocular Bevacizumab (Avastin®) compared with non-treatment control in patients with persistent diabetic macular edema or persistent active neovascularisat... | |||||||||||||
Medical condition: persistent diabetic macular edema or persistent active neovascularisation following lasercoagulation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
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 |
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