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Glaucoma, Open-Angle clinical trials

View clinical trials related to Glaucoma, Open-Angle.

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NCT ID: NCT05626426 Recruiting - Glaucoma Clinical Trials

Electrical Stimulation for the Treatment of Optic Neuropathies

rtACS
Start date: February 27, 2023
Phase: N/A
Study type: Interventional

The overall aim of this study is to see whether long-term electrical stimulation with a home-stimulation device works well and is safe for the treatment of open-angle glaucoma. Open-Angle Glaucoma is a disease where the nerves in the back of your eye die off faster than expected regardless of your eye pressure.

NCT ID: NCT05625958 Not yet recruiting - Clinical trials for Glaucoma, Open-Angle

Clinical Study Evaluating the Efficacy and Safety of CID v2.2 in Glaucoma Surgery

SAFARI4
Start date: March 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of implanting a new version of an interposition supraciliary implant (SV22) as a stand-alone therapy for lowering intraocular pressure (IOP) in patients with primary open and narrow angle glaucoma who have failed at least one class of topical medical therapy

NCT ID: NCT05624398 Recruiting - Cataract Clinical Trials

Results of Patients With Glaucoma Undergoing Minimally Invasive Glaucoma Surgery in Conjunction With Cataract Surgery

Start date: December 7, 2022
Phase: N/A
Study type: Interventional

This study is designed to determine how well patients with glaucoma can see following cataract surgery with a special type of lens called an extended-depth-of-focus (EDOF) lens. This lens is intended to reduced the patients need for glasses following cataract surgery. Patients will also undergo a minimally invasive type of glaucoma surgery using a special type of stent to reduce eye pressure, with the goal of better glaucoma control and the reduction in the need for medications to control eye pressure.

NCT ID: NCT05606796 Recruiting - Effect of Drug Clinical Trials

Comparison of Preserved and Preservative-free Latanoprost 0.005% in Primary Open Angle Glaucoma and Ocular Hypertensive Patients, at Guinness Eye Centre, Lagos.

Start date: December 2022
Phase: Phase 4
Study type: Interventional

It is a randomised, double-blinded clinical trial in which consenting participants who meet the inclusion criteria would be randomised into 2 groups. Subjects will be given either preserved or preservative free latanoprost for a period of 12 weeks. The efficacy and tolerability of both drugs would be assessed every 4 weeks, amongst these patients.

NCT ID: NCT05605743 Recruiting - Hypertension Clinical Trials

Alternate Nostril Breathing Training in Geriatrics With Glaucoma and High Blood Pressure

Start date: September 15, 2022
Phase: N/A
Study type: Interventional

Hypertension, particularly if poorly controlled, appears related to an increased risk of open angle glaucoma, (the high tension type of glaucoma is characterized as optic nerve degeneration with ocular hypertension). so this study will search response of glaucoma to breathing exercise

NCT ID: NCT05593354 Not yet recruiting - Glaucoma Clinical Trials

MicroPulse TLT - UK Study

MPTLTUKS
Start date: May 1, 2023
Phase:
Study type: Observational [Patient Registry]

This Prospective Interventional Study will assess the efficacy of MPTLT in the UK.

NCT ID: NCT05583591 Recruiting - Open Angle Glaucoma Clinical Trials

Combined Phacoemulsification With iStent Inject W Versus Hydrus for Mild to Moderate Open Angle Glaucoma

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The goal of the study is to prospectively evaluate and compare Hydrus microstent to the iStent Inject Wide in combination with cataract surgery in patients with mild to moderate open angle glaucoma. Hydrus and iStent are the two FDA approved trabecular meshwork targeting microstents to treat open angle glaucoma in conjunction with cataract surgery.

NCT ID: NCT05583474 Recruiting - Clinical trials for Open Angle Glaucoma or Ocular Hypertension

OPC-1085EL in the Treatment of Primary Open Angle Glaucoma or Ocular Hypertension in Chinese Subjects

Start date: September 27, 2022
Phase: Phase 3
Study type: Interventional

It is a phase III, multi-center, randomized, single-blind (to evaluator), parallel, and positive-controlled clinical trial evaluating the efficacy and safety of OPC-1085EL in the treatment of primary open angle glaucoma or ocular hypertension in Chinese subjects. It is planned that 240 subjects (120 in each group) will be randomly assigned to receive OPC-1085EL or 0.005% latanoprost ophthalmic solution (latanoprost) at a ratio of 1:1.

NCT ID: NCT05564091 Recruiting - Clinical trials for Primary Open Angle Glaucoma

Cataract Surgery in Conjunction With Ab-interno Canaloplasty Compared to Cataract Surgery Only in Patients With Mild to Moderate Primary Open-Angle Glaucoma

CATALYST
Start date: September 8, 2022
Phase: N/A
Study type: Interventional

A prospective, multicenter, randomized, single-masked, post-market clinical trial comparing cataract surgery in conjunction with ab-interno canaloplasty utilizing the iTrack Advance canaloplasty device (Nova Eye, Inc.) to cataract surgery only in patients with mild to moderate, primary open angle glaucoma. Subjects will be followed for 12 months.

NCT ID: NCT05557721 Enrolling by invitation - Clinical trials for Primary Open Angle Glaucoma

Uddevalla Skövde Transscleral Micropulse Study

USTMS
Start date: October 6, 2023
Phase:
Study type: Observational

Micro pulse transscleral laser treatment (MP-TLT) is a relatively new method to reduce the intraocular pressure (IOP) in glaucoma. New recommendations regarding the treatment protocol has recently been developed and was published 2022. The overall objective is to evaluate the efficacy and safety of the proposed treatment method in an independent study. In addition, the outcome of MP-TLT in patients with pseudoexfoliation glaucoma, which is relatively common in the Nordic countries, and primary open angle glaucoma will be studied separately. The IOP change over the course of one year will be monitored, as well as success rate and survival. Further, patient-reported discomfort from the treatment and the occurrence of any adverse events or complications will be studied.