- Trials with a EudraCT protocol (166)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
166 result(s) found for: Ocular hypertension.
Displaying page 7 of 9.
EudraCT Number: 2010-022586-10 | Sponsor Protocol Number: SCO 5511 | Start Date*: 2011-05-05 | |||||||||||
Sponsor Name:Alfred E. Tiefenbacher (GmbH & Co. KG) | |||||||||||||
Full Title: Randomized, Double-Masked, Active Controlled, Crossover Phase III Equivalence Study of Travoprost Eye Drops Solution in Subjects with Open Angle Glaucoma or Ocular Hypertension | |||||||||||||
Medical condition: Open Angle Glaucoma or Ocular Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009182-34 | Sponsor Protocol Number: DOR/2008 | Start Date*: 2009-03-30 | |||||||||||
Sponsor Name:ALFRED E. TIEFENBACHER (GMBH & CO. KG) | |||||||||||||
Full Title: RANDOMIZED, DOUBLE MASKED; ACTIVE CONTROLLED, CROSSOVER PHASE III EQUIVALENCE STUDY OF DORZOLAMIDE 2 % EYE DROPS SOLUTION IN SUBJECTS WITH OPEN ANGLE GLAUCOMA OR OCULAR HYPERTENSION | |||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004862-33 | Sponsor Protocol Number: BCBe/04/Neb-Gla/081 | Start Date*: 2006-05-23 |
Sponsor Name:Berlin-Chemie Menarini | ||
Full Title: INFLUENCE OF NEBIVOLOL ON OCULAR PERFUSION IN PATIENTS WITH ARTERIAL HYPERTENSION AND GLAUCOMA A mono-center, active-substance controlled, randomized, double-blind, prospective phase IV parallel-g... | ||
Medical condition: Arterial hypertension and glaucoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-015795-10 | Sponsor Protocol Number: SMA-09-19-SVN | Start Date*: 2009-11-12 |
Sponsor Name:Alcon d.o.o. | ||
Full Title: Assessing the safety and efficacy of switching to Azarga (Brinzolamide/Timolol Fixed Combination), as replacement therapy in patients with uncontrolled intraocular pressure | ||
Medical condition: uncontrolled intraocular pressure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001528-41 | Sponsor Protocol Number: PG324-CS303 | Start Date*: 2017-06-27 |
Sponsor Name:Aerie Pharmaceuticals Ireland Ltd. | ||
Full Title: A prospective, double-masked, randomized, multicenter, active-controlled, parallel-group, 6-month study assessing the safety and ocular hypotensive efficacy of PG324 Ophthalmic Solution compared to... | ||
Medical condition: Open angle glaucoma (OAG) or ocular hypertension (OHT) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) BE (Completed) AT (Completed) LV (Completed) HU (Completed) PL (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004587-29 | Sponsor Protocol Number: C11-034 | Start Date*: 2012-01-26 | |||||||||||
Sponsor Name:Alcon Research Ltd. | |||||||||||||
Full Title: A Multicenter, Double-Masked Study of the Safety and Efficacy of Travoprost Ophthalmic Solution, 0.003% Compared to TRAVATAN in Patients with Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||
Medical condition: Glaucoma; elevated Intraocular Pressure (IOP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) ES (Completed) AT (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000147-45 | Sponsor Protocol Number: YS001 | Start Date*: 2021-06-04 |
Sponsor Name:YONSUNG GMBH | ||
Full Title: A non-inferiority, randomized, investigator - masked, two-parallel group, phase III clinical trial, to evaluate the efficacy and safety of a preservative free formulation of latanoprost (YSLT) vers... | ||
Medical condition: GLAUCOMA, OCCULAR HYPERTENSION | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000961-10 | Sponsor Protocol Number: NITRO Protocol | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:Royal Liverpool and Broadgreen University Hospitals Trust | |||||||||||||
Full Title: Neoadjuvant IntraviTreal Ranibizumab treatment in high risk Ocular melanoma patients: A two stage single centre Phase II single arm study (NITRO Trial) | |||||||||||||
Medical condition: Uveal Melanoma (requiring enucleation) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015798-11 | Sponsor Protocol Number: 2452-001 | Start Date*: 2010-03-25 | ||||||||||||||||
Sponsor Name:Merck & Co., Inc. | ||||||||||||||||||
Full Title: Ensayo de fase III, aleatorizado, controlado con un fármaco de comparación activo, con doble enmascaramiento, de doce semanas de duración, para comparar la eficacia y la seguridad de MK-2452 (0,00... | ||||||||||||||||||
Medical condition: Glaucoma de ángulo abierto e hipertensión ocular /Open-Angle Glaucoma and Ocular Hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-004160-58 | Sponsor Protocol Number: CHASAP | Start Date*: 2021-06-11 | ||||||||||||||||
Sponsor Name:Centre hospitalier intercommunal de Créteil | ||||||||||||||||||
Full Title: Chronic Hypertension and Acetyl Salicylic Acid in Pregnancy, a multicenter prospective randomized double-blind placebo-controlled trial | ||||||||||||||||||
Medical condition: Pregnant women with chronic hypertension | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004841-34 | Sponsor Protocol Number: 101219 | Start Date*: 2020-08-24 | |||||||||||
Sponsor Name:Mika Harju | |||||||||||||
Full Title: Selective laser trabeculoplasty versus eye drops for first line treatment of exfoliation ocular hypertension or glaucoma: a randomised clinical trial | |||||||||||||
Medical condition: Glaucoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001733-41 | Sponsor Protocol Number: 004,1 | Start Date*: 2013-06-12 | ||||||||||||||||
Sponsor Name:Harju Mika | ||||||||||||||||||
Full Title: Hypertonic saline - the effect of repeating doses | ||||||||||||||||||
Medical condition: Elevated eyepressure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000552-18 | Sponsor Protocol Number: 769 | Start Date*: 2014-01-30 |
Sponsor Name:Bausch & Lomb Incorporated | ||
Full Title: A Randomized, Multicenter, Double-Masked, Parallel-Group Study Comparing the Safety and Efficacy of BOL-303259-X 0.024% (Latanoprostene Bunod) Ophthalmic Solution With Timolol Maleate Ophthalmic ... | ||
Medical condition: Open-Angle Glaucoma or Ocular Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-020213-82 | Sponsor Protocol Number: GLC-04-10 | Start Date*: 2010-05-27 | ||||||||||||||||||||||||||
Sponsor Name:IRCCS- FONDAZIONE G.B. BIETTI PER LO STUDIO E LA RICERCA IN OFTALMOLOGIA-ONLUS | ||||||||||||||||||||||||||||
Full Title: Comparison of Incidence and Severity of conjunctival hyperemia associated with use of topical Bimatoprost 0.01% and latanoprost 0.005% in Glaucoma or Ocular Hypertensive patients | ||||||||||||||||||||||||||||
Medical condition: glaucoma or ocular hypertension | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005540-34 | Sponsor Protocol Number: CLR_14_12 | Start Date*: 2016-07-19 | |||||||||||
Sponsor Name:Sun Pharma Advanced Research Company, Ltd. (SPARC) | |||||||||||||
Full Title: A Multi-Center, Investigator-Masked, Randomized, Crossover, Equivalence Study of the Safety and Efficacy of Once Daily Brimonidine Tartrate 0.35% Ophthalmic Suspension Compared with Brimonidine Tar... | |||||||||||||
Medical condition: Open-angle glaucoma, chronic angle closure glaucoma with patent iridotomy, pseudoexfoliation, pigment dispersion, or ocular hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000553-45 | Sponsor Protocol Number: 770 | Start Date*: 2013-09-13 |
Sponsor Name:Bausch & Lomb Incorporated | ||
Full Title: A Randomized, Multicenter, Double-Masked, Parallel-Group Study Comparing the Safety and Efficacy of BOL-303259-X 0.024% (Latanoprostene Bunod) Ophthalmic Solution With Timolol Maleate Ophthalmic ... | ||
Medical condition: Open-Angle Glaucoma or Ocular Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-000844-15 | Sponsor Protocol Number: A6111139 | Start Date*: 2008-10-29 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, NEW YORK, NY 10017. US | |||||||||||||
Full Title: A PHASE 1, OPEN-LABEL STUDY OF LATANOPROST ACID PLASMA CONCENTRATIONS IN PEDIATRIC AND ADULT GLAUCOMA PATIENTS TREATED WITH LATANOPROST 0.005% | |||||||||||||
Medical condition: GLAUCOMA | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) PT (Completed) DK (Completed) PL (Ongoing) IT (Completed) GR (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000963-25 | Sponsor Protocol Number: A1481156 | Start Date*: 2005-05-30 | |||||||||||
Sponsor Name:Pfizer Limited, Ramsgate Road, Sandwich, Kent, UK | |||||||||||||
Full Title: A Multicenter, Long-Term Extension Study to Assess Safety of Oral Sildenafil in the Treatment of Subjects Who Have Completed Study A1481131 | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) FI (Prematurely Ended) SK (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004201-29 | Sponsor Protocol Number: CM-05-08/HU | Start Date*: 2006-06-01 |
Sponsor Name:Alcon Hungarian ltd | ||
Full Title: THE EFFICACY AND SAFETY OF TIMOLOL MALEATE 0.5% COMPARED TO BRINZOLAMIDE 1% EACH GIVEN TWICE DAILY WHEN ADDED TO TRAVOPROST 0.004% GIVEN EACH EVENING IN PRIMARY OPEN-ANGLE GLAUCOMA OR OCULAR HYPERT... | ||
Medical condition: Increased intraocular pressure and glaucoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-002245-12 | Sponsor Protocol Number: EORTC 18021 | Start Date*: 2005-01-27 | |||||||||||
Sponsor Name:European Organisation for the Research and Treatment of Cancer | |||||||||||||
Full Title: Intravenous versus intra-arterial fotemustine chemotherapy in patients with liver metastases from uveal melanoma: a randomized phase III study of the EORTC Melanoma Group. | |||||||||||||
Medical condition: Uveal melanomas with specific hepatic tropism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
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