- Trials with a EudraCT protocol (32)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
32 result(s) found for: Cystoid macular edema.
Displaying page 1 of 2.
| EudraCT Number: 2007-000705-30 | Sponsor Protocol Number: KONK1001 | Start Date*: 2007-05-15 | |||||||||||
| Sponsor Name:Moorfields Eye Hospital Foundation Trust | |||||||||||||
| Full Title: efficacy of pegaptanib sodium (macugen) on uveitic cystoid macular oedema: an exploratory study | |||||||||||||
| Medical condition: uveitic cystoid macular oedema | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2008-004899-50 | Sponsor Protocol Number: 2200/07 | Start Date*: 2008-05-13 | ||||||||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
| Full Title: OCT analysis of cystoid macular edema in uveitis patients undergoing anti-inflammatory treatment | ||||||||||||||||||
| Medical condition: Cystoid macular edema in uveitis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-004416-35 | Sponsor Protocol Number: OFT-EDE-2016 | Start Date*: 2017-04-21 | |||||||||||
| Sponsor Name:Fundació Parc Taulí | |||||||||||||
| Full Title: Efficacy and safety of three regimens based on tobramycin, dexamethasone and diclofenac for the prevention of pseudophakic macular edema. Randomized clinical trial | |||||||||||||
| Medical condition: Pseudophakic macular edema is a pathology that results from cataract surgery, usually occurring 4-6 weeks after surgery, which directly affects the retina (specifically the macula, the region that ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| 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: 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: 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: 2012-004873-14 | Sponsor Protocol Number: NL_42463.068.12 | Start Date*: 2013-03-27 |
| Sponsor Name:University Eye Clinic Maastricht | ||
| Full Title: PREvention of Macular EDema after cataract surgery | ||
| Medical condition: Cystoid Macular Edema (CME) after cataract surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) HU (Completed) PT (Completed) DE (Completed) ES (Completed) BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002635-28 | Sponsor Protocol Number: OFT-Campos01-12 | Start Date*: 2013-04-19 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
| Full Title: ASSESSMENT OF THE EFFICACY OF SUBTENON NATURAL LEUCOCYTIC INTERFERON-α (IFNα) FOR THE TREATMENT OF DIABETIC MACULAR EDEMA (DME): A PILOT STUDY. | |||||||||||||
| Medical condition: DIABETIC MACULAR EDEMA (DME) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000237-17 | Sponsor Protocol Number: NL-80249 | Start Date*: 2022-12-15 |
| Sponsor Name: | ||
| Full Title: Prospective clinical trial to evaluate the efficacy of acetazolamide for the treatment of cystoid macular edema in inherited retinal dystrophies: the CAR trial | ||
| Medical condition: Cystoid Macular Edema in inherited retinal dystrophies | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2020-003408-15 | Sponsor Protocol Number: DMEC | Start Date*: 2021-06-14 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: A randomized clinical two-arm trial comparing inflammation and cystoid macular edema for the medication regimens postoperative topical NSAIDs and steroids to only postoperative topical steroids in ... | ||
| Medical condition: Corneal disease/opacification treated with corneal endothelial transplantation (DSAEK or DMEK surgery), and the medical treatment is anti-inflammatory eye drops to treat (and prevent) intraocular i... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-002526-43 | Sponsor Protocol Number: 150998-001 | Start Date*: 2012-01-30 | |||||||||||
| Sponsor Name:Allergan Limited | |||||||||||||
| Full Title: Single and Repeat Dose Study of the Safety and Efficacy of AGN-150998 in Patients with Exudative Age-related Macular Degeneration | |||||||||||||
| Medical condition: Exudative Age-related Macular Degeneration | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000385-22 | Sponsor Protocol Number: RF-2010-2318561 | Start Date*: 2014-10-07 | ||||||||||||||||
| Sponsor Name:Ospedale San Raffaele di Milano | ||||||||||||||||||
| Full Title: Nerve Growth Factor eye drops as a novel treatment for vision loss in patients with Retinitis Pigmentosa: from preclinical to clinical Phase II trial. | ||||||||||||||||||
| Medical condition: Retinitis pigmentosa with cystoid macular edema | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2006-005450-71 | Sponsor Protocol Number: LUZVT06 | Start Date*: 2007-06-29 |
| Sponsor Name:Augenklinik der LMU München | ||
| Full Title: INTRAVITREAL RANIBIZUMAB THERAPY FOR MACULA EDEMA SECONDARY TO CENTRAL RETINAL VEIN OCCLUSION (RAVO) | ||
| Medical condition: Macula edema resulting from central retinal vein occlusion in the eye | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-003232-21 | Sponsor Protocol Number: CLOUD | Start Date*: 2017-10-06 |
| Sponsor Name:Medizinische Universität Graz, Univers. Augenklinik | ||
| Full Title: EffiCacy and safety of topical ketoroLac trOmethamine and sUbtenon triamcinolone acetonideand a “watch-and-wait” strategy for acute pseudophakic macular eDema: a randomized phase-3 trial | ||
| Medical condition: Pseudophakic macular edema | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002666-47 | Sponsor Protocol Number: SOAP1 | Start Date*: 2017-11-02 | |||||||||||
| Sponsor Name:Dpt. of Ophthalmology, Rigshospitalet-Glostrup | |||||||||||||
| Full Title: Effect of drop-less surgery compared to topical NSAID alone and combination of steroid and NSAID on central macular thickness after cataract surgery, a randomized controlled trial | |||||||||||||
| Medical condition: Postoperative cystoid macular edema following cataract surgery | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: 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: 2010-018741-65 | Sponsor Protocol Number: OPH1001A | Start Date*: 2010-04-21 | ||||||||||||||||
| Sponsor Name:OPHTHOTECH CORPORATION | ||||||||||||||||||
| Full Title: A PHASE 2, RANDOMIZED, DOUBLE-MASKED, CONTROLLED TRIAL TO ESTABLISH THE SAFETY AND EFFICACY OF INTRAVITREOUS INJECTIONS OF E10030 (ANTI-PDGF PEGYLATED APTAMER) GIVEN IN COMBINATION WITH LUCENTIS® I... | ||||||||||||||||||
| Medical condition: Subfoveal choroidal neovascularization secondary to age-related macular degeneration (AMD) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: LV (Completed) FR (Completed) BE (Completed) DE (Completed) ES (Completed) HU (Completed) IT (Completed) AT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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