- 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 4 of 9.
EudraCT Number: 2004-002979-16 | Sponsor Protocol Number: SPON UWCM 014 | Start Date*: 2004-11-12 |
Sponsor Name:CARDIFF UNIVERSITY | ||
Full Title: A Six-Week/Six-Week, Prospective, Randomised, Masked, Cross over, Primary Therapy Study comparing IOP Lowering Effects of Lumigan® and Xalatan® in Subjects with Primary Open Angle Glaucoma, Ocular... | ||
Medical condition: Primary open-angle glaucoma, Ocular hypertension, Pseudoexfoliation glaucoma or Pigment dispersion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000160-34 | Sponsor Protocol Number: BECRO/OV/BRIMTIM | Start Date*: 2015-06-29 | |||||||||||||||||||||
Sponsor Name:OmniVision GmbH | |||||||||||||||||||||||
Full Title: Therapeutic Equivalence (non-inferiority), Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic Formulation of 0.2% Brimonidin... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002576-91 | Sponsor Protocol Number: Becro/OV/Travoprost | Start Date*: 2014-09-30 | |||||||||||||||||||||
Sponsor Name:OmniVision GmbH | |||||||||||||||||||||||
Full Title: Therapeutic Equivalence (non-inferiority), Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic Formulation of Travoprost 40μg... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-002910-29 | Sponsor Protocol Number: BECRO/PHN/LATANO | Start Date*: 2017-09-26 | |||||||||||||||||||||
Sponsor Name:PHARMATHEN | |||||||||||||||||||||||
Full Title: Therapeutic Equivalence (non-inferiority), Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic Preservative-Free Formulation ... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004524-29 | Sponsor Protocol Number: BECRO/PHN/LATIM | Start Date*: 2018-02-28 | |||||||||||||||||||||
Sponsor Name:PHARMATHEN | |||||||||||||||||||||||
Full Title: Therapeutic Equivalence (non-inferiority), Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic Preservative-Free Formulation ... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-001178-70 | Sponsor Protocol Number: BECRO/ACT/ORASIS-LT | Start Date*: 2023-01-26 | |||||||||||||||||||||
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/Timolol 0.05 mg/mL +... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004212-31 | Sponsor Protocol Number: CM-05-10 | Start Date*: 2007-12-20 | ||||||||||||||||||||||||||
Sponsor Name:Alcon Laboratories, Inc. | ||||||||||||||||||||||||||||
Full Title: A Double-Masked, Multiple-Dose, Study of the IOP-Lowering Efficacy of Brinzolamide 1.0% Compared to Placebo When Added to Travoprost 0.004%/Timolol 0.5% Fixed Combination as Adjunctive Therapy in P... | ||||||||||||||||||||||||||||
Medical condition: primary open-angle glaucoma exfoliation glaucoma pigmentary glaucoma ocular hypertension | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SI (Completed) CZ (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-010834-23 | Sponsor Protocol Number: C-09-006 | Start Date*: 2009-04-30 | |||||||||||
Sponsor Name:Alcon Research, Ltd. | |||||||||||||
Full Title: A multi-center, double-masked study of the safety and efficacy of DuoTrav APS compared to DuoTrav in patients with open-angle glaucoma or ocular hypertension | |||||||||||||
Medical condition: Open-angle glaucoma (with or without pseudoexfoliation or pigment dispersion component) or ocular hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001046-41 | Sponsor Protocol Number: 07OY004 | Start Date*: 2008-12-11 | |||||||||||
Sponsor Name:Nottingham University Hospital NHS Trust (Research & Development) | |||||||||||||
Full Title: Effectiveness of GANfort® in reducing intraocular pressure in patients presenting with significantly elevated intraocular pressure | |||||||||||||
Medical condition: Primary Open Angle Glaucoma Ocular Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004060-24 | Sponsor Protocol Number: Glaucoma Xalacam /Combigan | Start Date*: 2005-11-24 |
Sponsor Name:Department of Clinical Pharmacology | ||
Full Title: A double-masked randomized cross-over study comparing the effect of Xalacom (latanoprost/timolol) and Combigan (brimonidine/timolol) fixed combination on intraocular pressure and ocular blood flow ... | ||
Medical condition: Glaucoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000142-19 | Sponsor Protocol Number: VT-1201 | Start Date*: 2013-05-31 | |||||||||||
Sponsor Name:VISIOTACT PHARMA | |||||||||||||
Full Title: - | |||||||||||||
Medical condition: - | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003907-38 | Sponsor Protocol Number: DNB-001-CT001 | Start Date*: 2007-03-06 | |||||||||||
Sponsor Name:Danube Pharmaceuticals Inc. | |||||||||||||
Full Title: A Multi-Centre, Double-Blind, Randomised, Parallel-Group, Placebo Controlled Phase II Study to Investigate the Safety, Efficacy, and Pharmacokinetic Profile of Twice-daily DNB-001 in Previously Unt... | |||||||||||||
Medical condition: Intraocular hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003627-37 | Sponsor Protocol Number: IT-04-04 | Start Date*: 2006-09-22 | |||||||||||
Sponsor Name:ALCON ITALIA | |||||||||||||
Full Title: Hypotonic efficacy and tollerability of concomitant supply of Travoprost e Brinzolamide vs dorzolamide-timololo in fixed association in patient with glaucoma or ocular hypertension clinical study,... | |||||||||||||
Medical condition: Patient with glaucoma or ocular hypertension bilateral non controlled | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000913-35 | Sponsor Protocol Number: BECRO/OV/DORZO | Start Date*: 2019-05-21 | |||||||||||||||||||||
Sponsor Name:BECRO (Cyprus) Ltd | |||||||||||||||||||||||
Full Title: A Randomized, Observer-blind, two Parallel Group, Multi-center, Clinical Trial for Comparing the Efficacy and Tolerability of Dorzo-Vision® sine Preservative-Free Eye Drops vs. Trusopt® Preservativ... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002947-27 | Sponsor Protocol Number: SYL040012_IV | Start Date*: 2014-07-01 | |||||||||||
Sponsor Name:Sylentis S.A.U. | |||||||||||||
Full Title: A phase II, observer masked, active controlled study of SYL040012 for the treatment of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension (SYLTAG) | |||||||||||||
Medical condition: Open angle glaucoma - intraocular pressure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003979-18 | Sponsor Protocol Number: LT4030-301 | Start Date*: 2021-04-15 | |||||||||||
Sponsor Name:Laboratoires THEA | |||||||||||||
Full Title: Efficacy and Safety Assessment of T4030 Eye Drops versus Ganfort® UD in Ocular Hypertensive or Glaucomatous Patients. | |||||||||||||
Medical condition: Primary open-angle glaucoma or Ocular hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PL (Completed) HU (Completed) BG (Completed) BE (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002574-52 | Sponsor Protocol Number: 1698-301-007 | Start Date*: 2019-08-01 | ||||||||||||||||
Sponsor Name:Allergan Ltd. | ||||||||||||||||||
Full Title: A Phase 3b Study to Evaluate the Duration of Effect of Bimatoprost SR in Participants 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: GB (GB - no longer in EU/EEA) DE (Trial now transitioned) IE (Trial now transitioned) SE (Completed) CZ (Trial now transitioned) HU (Completed) PL (Trial now transitioned) DK (Trial now transitioned) BG (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005314-29 | Sponsor Protocol Number: QTM/OMN-0115 | Start Date*: 2016-03-02 |
Sponsor Name:OMNIVISION GmbH | ||
Full Title: Randomized, open-label, two parallel group clinical trial, conducted under blinding evaluator conditions to compare the efficacy and tolerability of preservative-free formulation of Latanoprost 50µ... | ||
Medical condition: Open Angle Glaucoma or Ocular Hypertension | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-005222-29 | Sponsor Protocol Number: LT2347-PIII-12/13 | Start Date*: 2014-12-19 | |||||||||||
Sponsor Name:Laboratoires THÉA | |||||||||||||
Full Title: Efficacy and Safety assessment of fixed combination unpreserved Latanoprost eye drops and Timolol 0.5% (T2347) versus Xalacom® in ocular hypertensive or glaucomatous patients. Phase III, internati... | |||||||||||||
Medical condition: glaucoma, ocular hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) ES (Completed) EE (Completed) HU (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000581-10 | Sponsor Protocol Number: 12OY006 | Start Date*: 2013-07-25 | |||||||||||
Sponsor Name:Nottingham University NHS Trust | |||||||||||||
Full Title: Evaluation of inflammatory markers in patients on topical anti-glaucoma drop therapy; a comparative trial of preserved and non-preserved primary medical treatment (eye drops) in patients with glauc... | |||||||||||||
Medical condition: Glaucoma is the condition that is being treated by these eye drops - however the study is aimed at measuring the amount of inflammation that develops on the surface of the eye when these drops are ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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