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Ocular Hypertension clinical trials

View clinical trials related to Ocular Hypertension.

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NCT ID: NCT05043831 Withdrawn - Ocular Hypertension Clinical Trials

Direct Selective Laser Trabeculoplasty in Ethnic Chinese Population The Zhuiguang Trial

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the effectiveness (Intra-Ocular Pressure lowering) and safety of Direct Selective Laser Trabeculoplasty (DSLT) in ethnic Chinese subjects with Primary Open Angle Glaucoma or Ocular Hypertension.

NCT ID: NCT04140279 Withdrawn - Ocular Hypertension Clinical Trials

A Study to Evaluate the Effect of Latanoprostene Bunod Ophthalmic Solution 0.024% on Episcleral Venous Pressure and Outflow Facility in Participants With Ocular Hypertension

Start date: May 13, 2022
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to determine the effect of latanoprostene bunod (LBN) ophthalmic solution 0.024% (a single dose and 7 days of once daily [QD] dosing) on 2 aspects of aqueous humor (AqH) dynamics (episcleral venous pressure [EVP] and outflow facility) in participants with ocular hypertension (OHT).

NCT ID: NCT04064918 Withdrawn - Clinical trials for OHT - Ocular Hypertension

Effects of Netarsudil and Timolol on Retinal Blood Vessel Density and Visual Acuity

Start date: December 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to compare the effect of Netarsudil and Timolol on eye pressure and blood vessels of the back of the eye.

NCT ID: NCT04005079 Withdrawn - Ocular Hypertension Clinical Trials

Pilocarpine After Combined Cataract/Trabectome Surgery

PACCT
Start date: June 5, 2019
Phase: Phase 3
Study type: Interventional

Combined cataract + trabectome surgery is a surgery designed to help lower the intraocular pressure (pressure in the eye) and hopefully reduce the need for topical drops, progression of glaucoma, and/or further glaucoma surgeries. The purpose of this study is to assess whether using pilocarpine, a medication which is FDA approved to induce miosis, (in other words cause the pupil to constrict or become smaller) provides additional benefit to the success of Trabectome and cataract surgery.

NCT ID: NCT03927443 Withdrawn - Ocular Hypertension Clinical Trials

A Comparative Study of SPARC's SDP-133 Once Daily and Lumigan in Subjects With Open Angle Glaucoma or Ocular Hypertension

Start date: June 10, 2019
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy of once daily dosing with SPARC's novel ophthalmic formulation of bimatoprost compared with Lumigan 0.01% in subjects with open-angle glaucoma or ocular hypertension.

NCT ID: NCT02623023 Withdrawn - Ocular Hypertension Clinical Trials

Prophylaxis for Anti-VEGF-induced IOP Elevation

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The purpose of our study is to determine the effect of prophylactic treatment with brimonidine/timolol fixed combination (Combigan®, Allergan; Dublin, IRL) or placebo therapy (Refresh tears®, Allergan; Dublin, IRL) on long-term IOP measurements in patients receiving serial intravitreal injection of 0.5 mg ranibizumab (0.05 mL) with six months follow-up. Intraocular pressure measurements will be correlated with changes on ancillary testing (Humphrey 24-2 visual field testing and optical coherence tomography (OCT) of the optic nerve head (ONH). Our study would be the first large, prospective, randomized double-blind placebo-controlled trial to examine the relationship between anti-vascular endothelial growth factor (VEGF) therapy and sustained ocular hypertension.

NCT ID: NCT02295358 Withdrawn - Ocular Hypertension Clinical Trials

The Effect of Omega-3 Fatty Acid Supplementation on Intraocular Pressure & Ocular Surface

Start date: November 2014
Phase: N/A
Study type: Observational

This study is designed with the intention to further elucidate the effects of omega-3 fatty acids on intraocular pressure (IOP) and signs/symptoms of dry eye. Prior studies have shown statistically significant lowering of IOP with use of omega-3 fatty acids but have only been performed in animal models. This study will be the first to attempt replication in human models. A limited number of studies have shown an increase in tear production/volume as well as a decrease in the subjective symptoms of dry eye, but more studies are needed to better define these effects. Better understanding of the effects of this supplement on intraocular pressure and dry eye will contribute to the expanding knowledge about the pathophysiology of glaucoma/ocular hypertension and dry eye syndrome and potentially lead to further studies about new potential treatment options for these conditions.

NCT ID: NCT01927406 Withdrawn - Glaucoma Clinical Trials

The Secondary Beneficial Effects of Prostaglandin Analog Treatment in Thyroid Eye Disease Patients.

Start date: June 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the potential secondary beneficial effect of prostaglandin analogues (PA) treatment in thyroid eye disease (TED) patients. This study aims to determine if PA would change the course of the orbitopathy in TED patients by altering the progression of the common features of TED, including fatty hypertrophy, proptosis, eyelid retraction and optic nerve compression. The eyes with thyroid eye disease and elevated intraocular pressure will be randomised to the PA treatment and the other eye will serve as a control eye and will be treated with Timolol.

NCT ID: NCT01721707 Withdrawn - Ocular Hypertension Clinical Trials

Latanoprost/Brinzolamide BID Versus Latanoprost BID in Patients With OAG or OH

Start date: December 2012
Phase: Phase 3
Study type: Interventional

This study is a double-masked, randomized, parallel group study in patients with open angle glaucoma or ocular hypertension. The aim of this study is to verify the efficacy of the fixed combination of Latanoprost 50 mcg / mL / brinzolamide 10mg/ml eye drops compared to Latanoprost 50μg/mL eye drops in reducing IOP

NCT ID: NCT01696383 Withdrawn - Glaucoma Clinical Trials

Assessing the Efficacy of DuoTrav as a Replacement Therapy in Glaucoma Patients in Russia

Start date: February 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of changing to DuoTrav® (Travoprost 0.004%/Timolol 0.5%) from prior prostaglandin analogue or beta-blocker monotherapy in Russian glaucoma patients with open-angle glaucoma or ocular hypertension whose intraocular pressure (IOP) is uncontrolled while on their current treatment.