- Trials with a EudraCT protocol (117)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
117 result(s) found for: Visual angle.
Displaying page 1 of 6.
EudraCT Number: 2011-002601-30 | Sponsor Protocol Number: QTM/OMN0111 | Start Date*: 2011-09-26 | |||||||||||
Sponsor Name:OMNIVISION GmbH | |||||||||||||
Full Title: A COMPARISON OF LATANOPROST 50µg/ml EYE DROPS vs. XALATAN EYE DROPS IN THE TREATMENT OF OPEN ANGLE GLAUCOMA: AN OPEN, RANDOMIZED, CLINICAL TRIAL | |||||||||||||
Medical condition: Open angle glaucoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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: 2009-010101-36 | Sponsor Protocol Number: Alcon SMA-08-22 | Start Date*: 2009-09-21 | |||||||||||||||||||||
Sponsor Name:Alcon Laboratories, Inc. | |||||||||||||||||||||||
Full Title: The Efficacy and Safety of Adding the Brinzolamide/Timolol Maleate Fixed Combination (Azarga®) to Prostaglandin Monotherapy | |||||||||||||||||||||||
Medical condition: primary open-angle glaucoma ocular hypertension pigment dispersion glaucoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-006005-61 | Sponsor Protocol Number: PRN 05-001 | Start Date*: 2006-03-16 | |||||||||||
Sponsor Name:Pharmaceutical Research Network, LLC | |||||||||||||
Full Title: A COMPARISON OF THE EFFICACY AND SAFETY OF THE DORZOLAMIDE/TIMOLOL FIXED COMBINATION GIVEN TWICE DAILY VERSUS THE LATANOPROST/TIMOLOL FIXED COMBINATION GIVEN ONCE EVERY MORNING FOLLOWING A RUN-IN... | |||||||||||||
Medical condition: open-angle glaucoma ocular hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2013-003083-31 | Sponsor Protocol Number: Becro/OV/Brimo | Start Date*: 2013-10-17 | ||||||||||||||||
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 Brimonidine 2 mg... | ||||||||||||||||||
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: 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: 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: 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: 2010-021039-14 | 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: 2022-004142-35 | Sponsor Protocol Number: ABSALON | Start Date*: 2023-04-18 | |||||||||||
Sponsor Name:Department of Ophthalmology, Rigshospitalet | |||||||||||||
Full Title: Additive Benefits of Semaglutide for open-AngLe glaucoma – an Opportunity for Neuroprotection (ABSALON) | |||||||||||||
Medical condition: mild and moderate glaucoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
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: 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: 2014-005273-37 | Sponsor Protocol Number: 201450 | Start Date*: 2015-02-17 | |||||||||||||||||||||
Sponsor Name:Santen Oy | |||||||||||||||||||||||
Full Title: A phase IV study on the changes in ocular signs and symptoms in patients with ocular hypertension or open-angle glaucoma switched from Ganfort® eye drops (bimatoprost 0.03%/timolol 0.5%) to Taptiq... | |||||||||||||||||||||||
Medical condition: Glaucoma or Ocular Hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FI (Completed) DE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004262-95 | Sponsor Protocol Number: 0130A01SA | Start Date*: 2019-01-07 | ||||||||||||||||
Sponsor Name:Santen SAS | ||||||||||||||||||
Full Title: Phase III, Multinational, Multicenter, Investigator-Masked, Randomised, Active-Controlled Trial, comparing the efficacy and safety of DE-130A with Xalatan® in Patients with Open-Angle Glaucoma or O... | ||||||||||||||||||
Medical condition: Open-Angle Glaucoma or Ocular Hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) GB (GB - no longer in EU/EEA) DE (Completed) EE (Completed) PL (Completed) ES (Completed) BE (Completed) AT (Completed) LV (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: 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: 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: 2009-010606-10 | Sponsor Protocol Number: C-09-001 | Start Date*: 2010-04-01 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: An Evaluation of Patient Reported Outcomes and Ocular Surface Health in Patients Using Travoprost APS Eye Drops Solution Versus XALATAN Eye Drops Solution | ||||||||||||||||||
Medical condition: Open Angle Glaucoma or Ocular Hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LT (Completed) IT (Completed) HU (Completed) BE (Completed) LV (Completed) SE (Completed) GB (Completed) | ||||||||||||||||||
Trial results: View results |
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