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Glaucoma clinical trials

View clinical trials related to Glaucoma.

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NCT ID: NCT04178863 Recruiting - Glaucoma; Drugs Clinical Trials

CATS Tonometer IOP Reduction Latanoprost Verses Timolol

Start date: July 1, 2018
Phase: Phase 4
Study type: Interventional

Topical Prostaglandin Analog vs Betablocker - Corneal Biomechanical Evaluation using CATS Tonometer Prism

NCT ID: NCT04172857 Completed - Glaucoma Secondary Clinical Trials

Treatment of Malignant Glaucoma by Anterior Vitrectomy From Two Different Approaches

Start date: May 1, 2015
Phase:
Study type: Observational

To compare the surgical outcomes of treating phacoemulsification with intraocular lens implantation combined with goniosynechialysis (Phaco-IOL-GSL) associated malignant glaucoma (MG), using different incision sites in anterior vitrectomy combined with hyaloidotomy, zonulectomy, and iridectomy (VHZI).

NCT ID: NCT04164459 Recruiting - Glaucoma Clinical Trials

Evaluating the Efficacy and Safety of Xalost S in Glaucoma Patients.

Start date: December 19, 2018
Phase: Phase 4
Study type: Interventional

In patients with Glaucoma, Xalost S or Xalatan or Taflotan-S are administered for 12 weeks. After 12 weeks, among them, Xalatan administration group are switched to Xalost S or Taflotan-S. Extension study period is 8 weeks. To compare effect (ocular surface damage) and safety of preservative-free Latanoprost/Tafluprost to Benzalkonium chloride-preserved Latanoprost in primary open angle glaucoma or normal tension glaucoma.

NCT ID: NCT04161963 Recruiting - Cataract Clinical Trials

Incidence of Sub-clinical Cystoid Macular Edema After Cataract Surgery

ICCME
Start date: March 4, 2019
Phase:
Study type: Observational

Cystoid macular edema (CME) can limit visual acuity after cataract surgery. Little is known whether the incidence is similar between standard ultrasound phacoemulsification cataract surgery (phaco), femtolaser assisted cataract surgery (FLACS), and combined phacoemulsification cataract surgery plus micro invasive glaucoma surgery (phaco+MIGS) procedures.

NCT ID: NCT04157530 Completed - Glaucoma Clinical Trials

Clinical Evaluation of Acupuncture in Treating Glaucoma

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The present study predicts that acupuncture or electroacupuncture can reduce intraocular pressure and also can improve quality of life in patients with glaucoma.

NCT ID: NCT04155164 Recruiting - Clinical trials for Primary Open Angle Glaucoma

Effect of Metformin on Visual Function in Patients With Glaucoma

Start date: December 10, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Metformin could prevent the progression of glaucoma in a safe and effective manner.

NCT ID: NCT04149899 Completed - Ocular Hypertension Clinical Trials

Safety and IOP-Lowering Effects of WB007

Start date: November 14, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The study evaluated the safety and IOP-lowering effects of WB007 in adults with primary open-angle glaucoma or ocular hypertension in both eyes. This was a 2-part study. Part 1 was a 3-period dose escalation that evaluated 3 concentrations of WB007 ophthalmic solution following a single dose in one eye. Part 2 was a randomized, double-masked, parallel comparison that evaluated two concentrations of WB007 (selected based on Part 1 results) in both eyes compared with timolol 0.5% for 14 days.

NCT ID: NCT04145830 Completed - Clinical trials for Glaucoma Treatment Using Focused Ultrasound

UCP Glaucoma Treatment for Primary Glaucoma in China

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

To collect safety and efficacy data on Ultrasound Cycle Plasty treatment (UCP) in primary glaucoma asian patients.

NCT ID: NCT04143620 Completed - Visual Impairment Clinical Trials

Triple Procedure for Dense Cataractus Neovascular Glaucoma Patients

NVG
Start date: July 1, 2016
Phase: N/A
Study type: Interventional

Background: One of the most difficult refractory glaucomas in treatment is the neovascular type and its association with dense cataract add to this difficulty. This study aimed to provide results of triple surgical treatment of such conditions. Methods: A total of 12 eyes of 12 patients with dense cataractus NVG patients were included in this study. The patients mean age was 57.25 ± 5.9 years. The mean pre-operative intraocular pressure (IOP) was 47.25 ± 4.04 mmHg with maximum antiglaucoma therapy. The mean best corrected distant visual acuities (BCDVA) in log MAR was 2.13 ± 0.38. All the patients received intra-vitreal injection of 1.25 mg (0.05 ml) bevacizumab followed by phacoemulsification, pars plana vitrectomy (PPV) including pan-retinal photocoagulation (PRP), and assisted trabeculectomy with Mitomycin c (MMC). Mean IOP and BCDVA changes were the main outcome results of this study.

NCT ID: NCT04141891 Completed - Stroke Clinical Trials

Advancing Understanding of Transportation Options

AUTO
Start date: December 12, 2019
Phase: N/A
Study type: Interventional

This Stage II randomized, controlled, longitudinal trial seeks to assess the acceptability, feasibility, and effects of a driving decision aid use among geriatric patients and providers. This multi-site trial will (1) test the driving decision aid (DDA) in improving decision making and quality (knowledge, decision conflict, values concordance and behavior intent); and (2) determine its effects on specific subpopulations of older drivers (stratified for cognitive function, decisional capacity, and attitudinally readiness for a mobility transition). The overarching hypotheses are that the DDA will help older adults make high-quality decisions, which will mitigate the negative psychosocial impacts of driving reduction, and that optimal DDA use will target certain populations and settings.