- Trials with a EudraCT protocol (85)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
85 result(s) found for: Glaucoma medication.
Displaying page 1 of 5.
EudraCT Number: 2010-022984-36 | Sponsor Protocol Number: 201051 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Santen Oy | ||||||||||||||||||||||||||||
Full Title: A phase III, randomized, double-masked 6-month clinical study to compare the efficacy and safety of the preservative-free fixed dose combination of tafluprost 0.0015% and timolol 0.5% eye drops to ... | ||||||||||||||||||||||||||||
Medical condition: Patients diagnosed with ocular hypertension or open-angle glaucoma (primary open-angle glaucoma [POAG], capsular glaucoma or pigmentary glaucoma). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: HU (Completed) LV (Completed) CZ (Completed) ES (Completed) PT (Completed) AT (Completed) BG (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000044-10 | Sponsor Protocol Number: QTM/OMN0114 | Start Date*: 2015-03-30 | ||||||||||||||||
Sponsor Name:OMNIVISION | ||||||||||||||||||
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: Open Angle Glaucoma or Ocular Hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002131-18 | Sponsor Protocol Number: 192024-093 | Start Date*: 2016-12-21 | |||||||||||||||||||||
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 and Ocular Hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) DK (Completed) PL (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002760-34 | Sponsor Protocol Number: C-08-10 | Start Date*: 2008-10-02 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: A Multi-Center, Double-Masked Study of the Safety and Efficacy of Travoprost APS Compared to TRAVATAN® in Patients 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: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020746-98 | Sponsor Protocol Number: 77557 | Start Date*: 2010-11-01 | ||||||||||||||||
Sponsor Name:Santen Oy | ||||||||||||||||||
Full Title: An open-label phase IV study on the changes in ocular signs and symptoms in patients with ocular hypertension or open-angle glaucoma switched from preserved travoprost 0.004% eye drops to preservat... | ||||||||||||||||||
Medical condition: Patients diagnosed with Ocular Hypertension or Open-angle glaucoma (primary open-angle glaucoma [POAG] or capsular glaucoma) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022965-82 | Sponsor Protocol Number: 201050 | Start Date*: 2010-12-22 | ||||||||||||||||||||||||||
Sponsor Name:Santen Oy | ||||||||||||||||||||||||||||
Full Title: A phase III, randomized, double-masked 6-month clinical study to compare the efficacy and safety of the preservative-free fixed-dose combination of tafluprost 0.0015% and timolol 0.5% eye drops to ... | ||||||||||||||||||||||||||||
Medical condition: Ocular hypertension and POAG, capsular glaucoma and pigmentary glaucoma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FI (Completed) GB (Completed) DE (Completed) EE (Completed) NL (Completed) PL (Completed) IT (Completed) BE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-005936-99 | Sponsor Protocol Number: C-07-16 | Start Date*: 2008-11-19 | |||||||||||
Sponsor Name:Alcon Research, Ltd. | |||||||||||||
Full Title: Effects of Topical Hypotensive Drugs on Circadian Ocular Perfusion Pressure and Ocular Blood Flow in Patients with Open-Angle Glaucoma | |||||||||||||
Medical condition: Open-Angle Glaucoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021039-14 | Sponsor Protocol Number: S001-2010 | Start Date*: 2010-08-19 | ||||||||||||||||
Sponsor Name:Tampere University, Faculty of Medicine, Department of Ophthalmology | ||||||||||||||||||
Full Title: An open-label, phase IV, pilot study, to evaluate confocal microscopic findings of cornea, ocular signs and symptoms in patients with ocular hypertension or open-angle glaucoma switching from latan... | ||||||||||||||||||
Medical condition: Ocular Hypertension (OH) or Open-Angle Glaucoma (OAG); primary open-angle glaucoma [POAG] or capsular glaucoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000161-13 | Sponsor Protocol Number: RDG-10-272 | Start Date*: 2012-03-07 | ||||||||||||||||
Sponsor Name:Alcon Research Ltd | ||||||||||||||||||
Full Title: Assessing the Efficacy and Tolerability of Changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5% BAK-Free Fixed Combination), as Replacement Therapy in Patients Previously on Bimatoprost 0.03%/Timol... | ||||||||||||||||||
Medical condition: The study population must have been diagnosed with 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: 2007-002501-45 | Sponsor Protocol Number: EMD-06-02 | Start Date*: 2008-03-14 | ||||||||||||||||
Sponsor Name:Alcon Laboratories Inc. | ||||||||||||||||||
Full Title: Phase IV randomised double masked clinical trial: Assessing morning versus evening dosing of a fixed dose combination of Travoprost 0.004% / Timolol Maleate 0.5% in patients with primary open angle... | ||||||||||||||||||
Medical condition: Open - angle glaucoma or ocular hypertension. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006027-31 | Sponsor Protocol Number: C-08-40 | Start Date*: 2009-04-16 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: A multi-center, double-masked study of the safety and efficacy of Travoprost APS compared to TRAVATAN in patients 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: BE (Completed) LV (Completed) FR (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022948-21 | Sponsor Protocol Number: RDG-10-246 | Start Date*: 2011-03-08 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: Eficacia y Seguridad de añadir Brinzolamida/Maleato de Timolol en combinación fija (Azarga ®) en pacientes con Hipertensión ocular o Glaucoma no controlados en Monoterapia de Prostaglandinas | ||||||||||||||||||
Medical condition: Hipertension ocular o glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021973-35 | Sponsor Protocol Number: RDG-10-243 | Start Date*: 2010-10-14 | |||||||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | |||||||||||||||||||||||
Full Title: Assessing the Safety and Efficacy of Changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5% Fixed Combination), as Replacement Therapy in Patients Uncontrolled on Bimatoprost 0.03%/Timolol 0.5% Thera... | |||||||||||||||||||||||
Medical condition: Open-angle glaucoma, ocular hypertension or pigment dispersion glaucoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) CZ (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-013178-42 | Sponsor Protocol Number: C-09-032 | Start Date*: 2009-07-31 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: A Twelve-Month Open-Label Safety Study of Polyquaternium-Preserved DuoTrav APS Dosed Once Daily in Patients 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: BE (Completed) LV (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-003617-42 | Sponsor Protocol Number: BP25466 | Start Date*: 2011-12-14 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: An adaptive, multi-center, randomized, investigator-masked, subject-masked, multiple-dose, placebo-controlled, parallel study to investigate efficacy, safety, tolerability and pharmacokinetics of... | ||||||||||||||||||
Medical condition: Primary open angle glaucoma or ocular hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) BG (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002895-42 | Sponsor Protocol Number: GITS2013_4.0 | Start Date*: 2013-10-10 | ||||||||||||||||
Sponsor Name:Region Västerbotten | ||||||||||||||||||
Full Title: Glaucoma Intensity Treatment Study – Intensive non-invasive glaucoma treatment vs conventional stepwise treatment – a prospective, randomized phase IV study of disease progression in glaucoma (GITS... | ||||||||||||||||||
Medical condition: Glaucoma, open-angle and PEX glaucoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010604-29 | Sponsor Protocol Number: C-09-007 | Start Date*: 2009-06-30 | ||||||||||||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||||||||||||
Full Title: An evaluation of the Ocular Surface Health in Subjects Using DuoTrav APS Eye Drops Solution Versus XALACOM® EYE Drops Solution | ||||||||||||||||||||||||||||
Medical condition: glaucoma/dry eye | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) HU (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) BE (Completed) PT (Prematurely Ended) AT (Prematurely Ended) GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-001128-35 | Sponsor Protocol Number: A6641038 | Start Date*: 2005-06-02 | |||||||||||
Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
Full Title: A 12-week randomised, evaluator-masked, parallel-group, multinational, multi-centre study comparing the efficacy and safety of the fixed combination of latanoprost and timolol (XalacomTM) with the ... | |||||||||||||
Medical condition: open angle glaucoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000736-15 | Sponsor Protocol Number: GLH694-P001 | Start Date*: 2015-09-14 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: Additive Effect of Twice Daily Brinzolamide 1% /Brimonidine 0.2% Fixed Dose Combination as an Adjunctive Therapy to a Prostaglandin Analogue | ||||||||||||||||||
Medical condition: Ocular Hypertension Open-angle Glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) ES (Completed) GB (Completed) FR (Completed) GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000176-20 | Sponsor Protocol Number: GLJ576-P001 | Start Date*: 2016-05-29 | ||||||||||||||||
Sponsor Name:Alcon Research Ltd | ||||||||||||||||||
Full Title: Safety and Efficacy with Twice Daily Brinzolamide 1% / Brimonidine 0.2% (SIMBRINZA) as an Adjunctive Therapy to Travoprost 0.004% / Timolol 0.5% (DUOTRAV) | ||||||||||||||||||
Medical condition: Ocular Hypertension Open-angle Glaucoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) BE (Completed) GB (Prematurely Ended) DE (Completed) GR (Completed) FR (Completed) NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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