- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Phacoemulsification.
Displaying page 1 of 2.
EudraCT Number: 2009-017031-18 | Sponsor Protocol Number: OZR-2009-06 | Start Date*: 2010-04-09 |
Sponsor Name:Rotterdam Eye Hospital | ||
Full Title: Treatment of Cystoid Macular Edema following cataract surgery. A randomized, double-masked, placebo-controlled, clinical trial. | ||
Medical condition: cystoid macular edema | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003305-13 | Sponsor Protocol Number: 033/SI | Start Date*: 2006-08-01 | |||||||||||
Sponsor Name:SIFI | |||||||||||||
Full Title: Efficacy and safety of topical steroid/antibiotic association treatments following phacoemulsification cataract extraction | |||||||||||||
Medical condition: post-operative inflammation of eye anterior segment in the presence or at risk of bacterial infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005576-33 | Sponsor Protocol Number: LT2380-PII-09/12 | Start Date*: 2013-09-03 |
Sponsor Name:Laboratoires Théa | ||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) to obtain mydriasis in patients with small pupils for cataract surgery by phacoe... | ||
Medical condition: The primary aim of this study is to evaluate mydriasis obtained with T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) in patients with small pupils | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001660-30 | Sponsor Protocol Number: CHL.3/01-2019/M | Start Date*: 2020-06-03 | |||||||||||
Sponsor Name:Sintetica S.A. | |||||||||||||
Full Title: A prospective, observer-masked, randomized clinical trial to investigate and compare the clinical efficacy of chloroprocaine 3% gel and tetracaine 0.5% eye drop as topical anesthetics in phacoemuls... | |||||||||||||
Medical condition: cataract surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 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: 2010-019246-11 | Sponsor Protocol Number: 577 | Start Date*: 2010-07-15 | |||||||||||
Sponsor Name:Bausch & Lomb Incorporated | |||||||||||||
Full Title: A Randomized, Multicenter, Double-Blind, Parallel-Group Clinical Safety and Efficacy Evaluation of Loteprednol Etabonate Ophthalmic Gel, 0.5% versus Vehicle for the Treatment of Inflammation and Pa... | |||||||||||||
Medical condition: Inflammation and pain following cataract surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011913-26 | Sponsor Protocol Number: 588 | Start Date*: 2010-03-10 | |||||||||||
Sponsor Name:Dr. Gerhard Mann chem.-pharm Fabrik GmbH | |||||||||||||
Full Title: A Randomized, Multicenter, Double-Masked, Parallel-Group Dose Ranging Clinical Safety and Efficacy Evaluation of BOL-303242-X Ophthalmic Suspension versus Vehicle for the Treatment of Inflammation ... | |||||||||||||
Medical condition: inflammation of the eye follwoing cataract surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005287-24 | Sponsor Protocol Number: BAR104 | Start Date*: 2005-06-28 |
Sponsor Name:Univ.-Kl. f.Augenheilkunde und Optometrie Wien | ||
Full Title: Effect of diclofenac-sodium, unpreserved diclofenac-sodium or ketorolac on the inflammatory response after cataract surgery | ||
Medical condition: intraocular inflammatory reaction after cataract-surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021061-72 | Sponsor Protocol Number: 103462 | Start Date*: 2011-01-03 |
Sponsor Name:Ögonkliniken, Akademiska sjukhuset i Uppsala | ||
Full Title: To evaluate the safety and efficacy of a single subconjunctival injection of methylprednisolone versus standard postoperative steroid regiment in terms of intraocular inflammation and intraocular p... | ||
Medical condition: Att studera säkerheten och effekten av en engångs subkonjunktival injektion med metylprednisolon jämfört med sedvanliga postoperativa kortisonbehandling med ögondroppar avseende intraokulär tryckst... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
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: 2008-003279-28 | Sponsor Protocol Number: LT2380-PII-11/07 | Start Date*: 2008-07-24 | |||||||||||||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||||||||||||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) for anaesthesia and mydriasis in phacoemulsification cataract surgery | |||||||||||||||||||||||
Medical condition: The aim of the development was to develop a combination of active substances enabling to obtain at the same time a mydriasis and an anaesthesia during cataract surgery. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Ongoing) ES (Ongoing) BE (Completed) PT (Completed) | |||||||||||||||||||||||
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: 2010-019507-28 | Sponsor Protocol Number: C-09-055 | Start Date*: 2010-10-15 |
Sponsor Name:Alcon Research, Ltd. | ||
Full Title: Clinical Evaluation of Nepafenac Ophthalmic Suspension, 0.3% for Prevention and Treatment of Ocular Inflammation and Pain after Cataract Surgery | ||
Medical condition: The Prevention and Treatment of Ocular Inflammation and Pain after Cataract Surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) SE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021188-34 | Sponsor Protocol Number: LT2380-PIII-05/10 | Start Date*: 2011-07-01 | |||||||||||||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||||||||||||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaine, phenylephrine and tropicamide) for mydriasis and anaesthesia in phacoemulsification cataract surgery | |||||||||||||||||||||||
Medical condition: The aim of this clinical study will be to develop a combination of active substances enabling to obtain at the same time a mydriasis and an anaesthesia during cataract surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PT (Completed) DE (Completed) BE (Completed) AT (Completed) ES (Ongoing) SE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001149-15 | Sponsor Protocol Number: LevoDesa_05-2017 | Start Date*: 2018-07-31 | |||||||||||
Sponsor Name:NTC SRL | |||||||||||||
Full Title: Aqueous humour concentrations after topical apPlication of combinEd levofloxacin dexamethasone eye dRops and of its single components: a randoMized, assEssor-blinded, parallel-group study in patien... | |||||||||||||
Medical condition: Patients for which cataract surgery has been planned. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001362-32 | Sponsor Protocol Number: Prot-06032007 | Start Date*: 2008-03-03 | |||||||||||
Sponsor Name:University Hospitals Of Leicester NHS Trust | |||||||||||||
Full Title: The use of non-ionic contrast media to clear corneal scars | |||||||||||||
Medical condition: Will plan to investigate patients who would benefit from cataract surgery but whom have corneal scarring which would make surgery difficult. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004890-21 | Sponsor Protocol Number: NL72427.068.19 | Start Date*: 2021-01-18 |
Sponsor Name:Academic Hospital Maastricht (azM) | ||
Full Title: Effectiveness of Periocular drug Injection in CATaract surgery | ||
Medical condition: cystoid macular edema (CME) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) PT (Prematurely Ended) | ||
Trial results: View results |
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