- Trials with a EudraCT protocol (147)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18)
147 result(s) found for: Glaucoma, Open-Angle.
Displaying page 3 of 8.
EudraCT Number: 2014-003037-26 | Sponsor Protocol Number: 192024-091 | Start Date*: 2015-03-16 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: The Efficacy and Safety of Bimatoprost SR in Patients With Open-angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: Open-angle Glaucoma and Ocular Hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) AT (Completed) BE (Completed) ES (Completed) DK (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003597-26 | Sponsor Protocol Number: 1698-302-007 | Start Date*: 2019-11-07 | ||||||||||||||||
Sponsor Name:Allergan Ltd. | ||||||||||||||||||
Full Title: An Extension Trial to Evaluate the Long-term Safety and Efficacy of Bimatoprost SR in Patients with Open Angle Glaucoma or Ocular Hypertension | ||||||||||||||||||
Medical condition: Open-angle Glaucoma and Ocular Hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) AT (Prematurely Ended) DE (Ongoing) BE (Completed) ES (Ongoing) IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003631-34 | Sponsor Protocol Number: 192024-095 | Start Date*: 2017-01-12 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: A Comparison of Bimatoprost SR to Selective Laser Trabeculoplasty in Patients with Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: Open-angle glaucoma (OAG) or Ocular hypertension (OHT) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) ES (Temporarily Halted) CZ (Completed) FR (Completed) DK (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004307-14 | Sponsor Protocol Number: BECRO/ACT/LATANOS | Start Date*: 2021-02-12 | ||||||||||||||||
Sponsor Name:actrevo GmbH | ||||||||||||||||||
Full Title: Non-inferiority, Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic BAC-free Formulation of Latanoprost 0.05 mg/mL eye drops... | ||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension Elevated IOP and paediatric glaucoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004023-38 | Sponsor Protocol Number: GLC0107 | Start Date*: 2007-07-30 | |||||||||||
Sponsor Name:IRCCS- FONDAZIONE G.B. BIETTI PER LO STUDIO E LA RICERCA IN OFTALMOLOGIA-ONLUS | |||||||||||||
Full Title: Prospective, multicentric, double-masked clinical study to compare the efficacy and safety of Ganfort and Duotrav in primary open angle and pseudoexfoliative glaucoma patients previously treated wi... | |||||||||||||
Medical condition: Glaucoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003816-21 | Sponsor Protocol Number: RDG-10298 | Start Date*: 2012-01-11 | ||||||||||||||||
Sponsor Name:S.A. Alcon-Couvreur N.V | ||||||||||||||||||
Full Title: Multi-Center Study Assessing Efficacy and Tolerability of TRAVATAN® Solution without BAK, containing Polyquad® Preservative (0.004% travoprost) in Patients Previously on latanoprost 0.005% or bimat... | ||||||||||||||||||
Medical condition: Open angle Glaucoma Ocular Hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) SE (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
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: 2018-001727-39 | Sponsor Protocol Number: POP03 | Start Date*: 2018-10-16 | ||||||||||||||||
Sponsor Name:Polpharma S.A. | ||||||||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSSOVER, COMPARATIVE, NON-INFERIORITY TRIAL EVALUATING THE EFFICACY AND TOLERABILITY OF GENERIC LATANOPROST 0.05 MG/ML EYE DROPS SOLUTIO... | ||||||||||||||||||
Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-003387-27 | Sponsor Protocol Number: 848300145/0129/1POP04 | Start Date*: 2021-11-02 | ||||||||||||||||
Sponsor Name:Pharmaceutical Works Polpharma S.A. (Polpharma S. A.) | ||||||||||||||||||
Full Title: A PHASE III, MULTICENTRE, RANDOMISED, INVESTIGATOR-MASKED, CROSS-OVER, COMPARATIVE, NON-INFERIORITY TRIAL OF GENERIC LATANOPROST + TIMOLOL (50μG + 5MG)/ML EYE DROPS, SOLUTION (POLPHARMA S.A.) COMPA... | ||||||||||||||||||
Medical condition: Ocular hypertension and open angle glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002750-38 | Sponsor Protocol Number: C-08-09 | Start Date*: 2008-10-22 | |||||||||||||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||||||||||||
Full Title: 24-hour IOP control with Travoprost / Brinzolamide fixed combination once-daily (QD)in the evening vs TRAVATAN | |||||||||||||||||||||||
Medical condition: Open-angle 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: 2007-000515-29 | Sponsor Protocol Number: EMD-06-03 | Start Date*: 2007-07-04 | ||||||||||||||||
Sponsor Name:Alcon Laboratories Inc. | ||||||||||||||||||
Full Title: Adherencia de los pacientes en el uso de Travalert® para la instilación de una combinación fija de travoprost 0.004% / timolol 0.5% comparado con un régimen concomitante de travoprost 0.004% y timo... | ||||||||||||||||||
Medical condition: Reducción de la presión intraocular en pacientes con glaucoma de angulo abierto o con hipertensión ocular, que no respondan a monoterapia de betabloqueantes o análogos de las prostaglandinas Intr... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003186-24 | Sponsor Protocol Number: 192024-092 | Start Date*: 2015-04-23 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: The Efficacy and Safety of Bimatoprost SR in Patients With Open-angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: Open-angle Glaucoma and Ocular Hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) DE (Trial now transitioned) IT (Completed) NL (Completed) PT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-003089-42 | Sponsor Protocol Number: OPHT-250719 | Start Date*: 2019-12-23 | |||||||||||
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | |||||||||||||
Full Title: The effect of Tetrahydrocannabinol on ocular hemodynamics in patients with primary open angle glaucoma- A Phase II Study | |||||||||||||
Medical condition: The study will be carried out in patients with primary open angle glaucoma and healthy subjects | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002780-13 | Sponsor Protocol Number: C-07-63 | Start Date*: 2008-09-04 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Three-Month, Multicenter, Double-Masked Study Comparing the Safety and Efficacy of the Fixed Combination Travoprost + Brinzolamide Eye Drops, Suspension vs Travatan vs Azopt in Patients with Open... | ||||||||||||||||||||||||||||||||||||||
Medical condition: open-angle glaucoma or ocular hypertension | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) DE (Prematurely Ended) ES (Completed) BE (Completed) HU (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) PT (Prematurely Ended) AT (Prematurely Ended) LV (Completed) SE (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005091-42 | Sponsor Protocol Number: 192024-041D | Start Date*: 2012-05-08 | |||||||||||||||||||||
Sponsor Name:Allergan Limited | |||||||||||||||||||||||
Full Title: An Open Label (Stage 1) and Randomized (Stage 2), 24-Month Study of Safety and Efficacy of Bimatoprost Drug Delivery System in Patients With Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
Medical condition: open-angle glaucoma (OAG) and ocular hypertension (OHT) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000026-22 | Sponsor Protocol Number: QTM/OMN0112 | Start Date*: 2012-07-23 | ||||||||||||||||
Sponsor Name:Omnivision GmbH | ||||||||||||||||||
Full Title: Open, Observer-blind, two Parallel Group, Randomized, Multicentric Clinical Phase III Trial on the Comparison of Efficacy and Tolerability of a New Preservative-free Formulation of Travoprost 40 µg... | ||||||||||||||||||
Medical condition: Primary open angle glaucoma or intraocular hypertension | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005339-15 | Sponsor Protocol Number: QTM/OMN0211 | Start Date*: 2012-02-03 | ||||||||||||||||
Sponsor Name:Omnivision GmbH | ||||||||||||||||||
Full Title: Open, Observer-blind, two Parallel Group, Randomized, Multicentric Clinical Phase III Trial on the Comparison of Efficacy and Tolerability of a New Preservative-free Formulation of the Fixed Combin... | ||||||||||||||||||
Medical condition: Primary open angle glaucoma or intraocular hypertension | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024512-34 | Sponsor Protocol Number: C-10-040 | Start Date*: 2011-05-17 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: Safety and IOP-Lowering Efficacy of Brinzolamide 10 mg/ml / Brimonidine 2 mg/ml Fixed Combination Eye Drops, Suspension compared to Brinzolamide 10 mg/ml Eye Drops, Suspension and Brimonidine 2 mg/... | ||||||||||||||||||
Medical condition: Open-angle glaucoma and ocular hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) PT (Completed) LV (Completed) DE (Completed) HU (Completed) LT (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004872-37 | Sponsor Protocol Number: 77552 | Start Date*: 2007-11-21 |
Sponsor Name:Santen Oy | ||
Full Title: A phase IIIb study on the changes in ocular signs, symptoms and conjunctival inflammatory markers in patients with ocular hypertension or primary open-angle glaucoma switched from preserved latanop... | ||
Medical condition: Ocular hypertension or open angle glaucoma patients are enrolled into this trial. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) SE (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005607-18 | Sponsor Protocol Number: OPHT-011007 | Start Date*: 2009-04-02 | ||||||||||||||||
Sponsor Name:Ursapharm Arzneimittel GmbH & Co KG | ||||||||||||||||||
Full Title: An open study comparing the effects of moxaverine on ocular blood flow in patients with age- related macular degeneration, primary open angle glaucoma and healthy control subjects | ||||||||||||||||||
Medical condition: glaucoma age-related macular degeneration | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: View results |
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