- Trials with a EudraCT protocol (45)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
45 result(s) found for: Intraocular lens.
Displaying page 1 of 3.
EudraCT Number: 2013-003885-15 | Sponsor Protocol Number: OMS302-ILR-006 | Start Date*: 2014-01-06 | |||||||||||
Sponsor Name:Omeros Corporation | |||||||||||||
Full Title: A Phase 3 Randomised, Double-Masked, Placebo-Controlled Study of the Effect of OMS302 on Intraoperative Pupil Diameter in Subjects at High Risk of Intraoperative Floppy Iris Syndrome Undergoing Int... | |||||||||||||
Medical condition: Intraocular Lens Replacement (ILR) in subject at high risk for Intraoperative Floppy Iris Syndrome (IFIS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000867-25 | Sponsor Protocol Number: OMS302-ILR-004 | Start Date*: 2012-07-23 | |||||||||||
Sponsor Name:Omeros Corporation | |||||||||||||
Full Title: A Phase 3 Randomised, Double-Masked, Placebo-Controlled Study of the Pharmacokinetics of OMS302 and the Effect of OMS302 on Intraoperative Pupil Diameter and Early Postoperative Pain in Subjects Un... | |||||||||||||
Medical condition: Intraocular Lens Replacement with Pharmacoemulsification | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020932-20 | Sponsor Protocol Number: D4250C00001 | Start Date*: 2010-10-05 | ||||||||||||||||
Sponsor Name:AstraZeneca AB | ||||||||||||||||||
Full Title: A Double Masked, Placebo Controlled, Randomised, Parallel Group Phase IIa Study to assess the Tolerability, Safety, and Efficacy of AZD4017 for Raised Intra-Ocular Pressure | ||||||||||||||||||
Medical condition: Raised Intra-Ocular Pressure or primary open angle glaucoma (POAG) on anti-glaucoma monotherapy that has been stable in dose for at least 30 days prior to screening. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001855-10 | Sponsor Protocol Number: SNAP1 | Start Date*: 2019-01-22 | |||||||||||
Sponsor Name:Department of Ophtalmology, Rigshospitalet-Glostrup | |||||||||||||
Full Title: Steroids and Non-steroidal Anti-inflammatory drugs in the Postoperative regime after trabeculectomy. An investigator-initiated randomized study (The SNAP study) | |||||||||||||
Medical condition: Medically uncontrolled glaucoma that requires filtration surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000397-45 | Sponsor Protocol Number: OY060301 | Start Date*: 2005-06-02 |
Sponsor Name:Queen's Medical centre | ||
Full Title: Randomised Controlled Trial Of Intravitreal Triamcinolone In Patients With Diabetic Macular Oedema Refractory To Laser Treatment | ||
Medical condition: Diabetic macular oedema affecting vision and refractory to laser treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003407-34 | Sponsor Protocol Number: pre-CIN | Start Date*: 2021-06-01 |
Sponsor Name:Oslo University Hospital | ||
Full Title: A randomized clinical three-arm trial comparing inflammation and cystoid macular edema for the medication regimens preoperative and postoperative topical NSAIDs to only postoperative topical NSAIDs... | ||
Medical condition: Cataract surgery, and the medical treatment is anti-inflammatory eye drops to treat (and prevent) intraocular inflammation and development og cystoid macular edema. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002339-23 | Sponsor Protocol Number: MydriasisbeiMydrane | Start Date*: 2019-10-24 |
Sponsor Name:Medical University Graz, Department of Ophtalmology | ||
Full Title: Prospective intraindividual comparison of the mydriasis of a standardized intracameral anaesthetics with the topical preoperative drop application in the uncomplicated cataract surgery | ||
Medical condition: patients who need a cataract surgery in both eyes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
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: 2004-005015-29 | Sponsor Protocol Number: GS101-P2-CG | Start Date*: 2005-08-03 |
Sponsor Name:Les Laboratoires CTRS | ||
Full Title: A multicenter double-blind randomized study to investigate the efficacy and tolerability of three doses of GS-101 eye drops, an antisense oligonucleotide, versus placebo on inhibition of corneal ne... | ||
Medical condition: Patients suffering from keratitis or keratouveitits of infectious origin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-001324-34 | Sponsor Protocol Number: C-12-008 | Start Date*: 2013-03-07 |
Sponsor Name:Alcon Research Ltd | ||
Full Title: A 3 Month, Multicenter, Double-Masked Safety and Efficacy Study of Travoprost Ophthalmic Solution, 0.004% Compared to Timolol (0.5% or 0.25%) in Pediatric Glaucoma Patients | ||
Medical condition: Pediatric glaucoma;elevated intraocular pressure | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) PL (Completed) DE (Completed) PT (Completed) NL (Completed) ES (Completed) | ||
Trial results: View results |
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: 2017-003277-34 | Sponsor Protocol Number: T2380-PIV-017 | Start Date*: 2018-01-15 | ||||||||||||||||
Sponsor Name:Laboratoires Théa | ||||||||||||||||||
Full Title: Phase IV, open-label, randomized clinical trial to evaluate the effects of Fydrane® and standard topical mydriatics and anaesthetics protocol on ocular surface after cataract surgery. | ||||||||||||||||||
Medical condition: Cataracts | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010536-17 | Sponsor Protocol Number: C-09-003 | Start Date*: 2009-08-31 | ||||||||||||||||
Sponsor Name:ALCON RESEARCH, LTD. | ||||||||||||||||||
Full Title: A Clinical Safety and Efficacy Comparison of NEVANAC® 0.1% to Vehicle Following Cataract Surgery in Diabetic Retinopathy Patients | ||||||||||||||||||
Medical condition: macular edema following cataract surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) FR (Completed) DE (Completed) ES (Prematurely Ended) AT (Prematurely Ended) NL (Completed) IT (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004686-18 | Sponsor Protocol Number: 539 | Start Date*: 2008-02-08 |
Sponsor Name:Bausch&Lomb Dr Gerhard Mann chem.-Fabrik GmbH | ||
Full Title: A multicenter, Investigator-Masked, Parallel Group, Randomized, Study of the Efficacy and Safety of Indomethacin 0.1% Eyedrops Compared with Ketorolac 0.5% Eyedrops in the Ocular Inflammation After... | ||
Medical condition: Prevention of ocular inflammation in adults patients undergoing cataract surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) PT (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003029-40 | Sponsor Protocol Number: IOBA-01-2016 | Start Date*: 2017-02-14 |
Sponsor Name:IOBA - University of Valladolid | ||
Full Title: Phase II safety assessment of intravitreal injection of mesenchymal stem cells for acute non arteritic anterior ischemic optic neuropathy (NAION) | ||
Medical condition: Non arteritic anterior ischemic optic neuropathy (NAION) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002647-35 | Sponsor Protocol Number: C-04-65 | Start Date*: 2005-10-06 |
Sponsor Name:Alcon Research, Ltd | ||
Full Title: Nepafenac 0.1% Eye Drops, Suspension Compared to Ketorolac Trometamol 0.5% Eye Drops, Solution and Placebo (Nepafenac Vehicle) for the Prevention and Treatment of Ocular Inflammation and Ocular Pai... | ||
Medical condition: ocular pain and inflammation associated with cataract extraction and intraocular lens implantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) GB (Completed) ES (Completed) IT (Completed) PT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000292-33 | Sponsor Protocol Number: HGC_SAR_1_13 | Start Date*: 2013-11-07 | ||||||||||||||||
Sponsor Name:Laura Sararols Ramsay | ||||||||||||||||||
Full Title: Comparative study of the mydriatic effect of Mydriasert vs the use of topical instillation of phenylephrine (10%) and tropicamide (1%) before catarcat surgery. | ||||||||||||||||||
Medical condition: Cataract surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000624-37 | Sponsor Protocol Number: CLOBOF3-17IA03 | Start Date*: 2022-10-05 | ||||||||||||||||
Sponsor Name:Laboratorios Salvat, S.A. | ||||||||||||||||||
Full Title: A Phase 3, multicenter, randomized, evaluator-blinded clinical trial to assess the safety and efficacy of Clobetasol propionate ophthalmic nanoemulsion, 0.05% compared to Prednisolone acetate, 1% i... | ||||||||||||||||||
Medical condition: Inflammation and pain associated with ocular surgery. | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001874-12 | Sponsor Protocol Number: C-12-071 | Start Date*: 2013-11-07 |
Sponsor Name:Alcon Research, Ltd | ||
Full Title: Randomized, Double-Masked, Vehicle Controlled, Clinical Evaluation To Assess The Safety And Efficacy Of Nepafenac Ophthalmic Suspension, 0.3% For Improvement In Clinical Outcomes Among Diabetic Sub... | ||
Medical condition: Cataract surgery in diabetic patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) IT (Completed) DE (Completed) AT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001622-29 | Sponsor Protocol Number: ALI-P01-21-006 | Start Date*: 2023-03-01 | |||||||||||
Sponsor Name:Alimera Sciences Europe Limited | |||||||||||||
Full Title: A NON-RANDOMISED, OPEN-LABEL, UNCONTROLLED, MULTI-CENTRE, PHASE IIIB STUDY EVALUATING THE SAFETY AND EFFICACY OF FLUOCINOLONE ACETONIDE 190 MICROGRAMS INTRAVITREAL IMPLANT IN PAEDIATRIC SUBJECTS FR... | |||||||||||||
Medical condition: Non-Infectious Uveitis affecting the posterior segment | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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