Clinical Trials Logo

Glaucoma clinical trials

View clinical trials related to Glaucoma.

Filter by:

NCT ID: NCT00698945 Completed - Ocular Hypertension Clinical Trials

Comparison of Istalolâ„¢ 0.5% QD (Timolol Maleate/Sorbitol Complex, ISTA Pharmaceutical) to Brimonidine Tartrate 0.1% BID as Adjunctive Therapy to Latanoprost 0.005% in Adults With Ocular Hypertension (OHT) or Open-Angle Glaucoma (OAG)

Start date: June 2008
Phase: Phase 4
Study type: Interventional

To assess the additional benefit of common adjunctive classes on the diurnal IOP curve in patients assessed as needing additional treatment to reach target intraocular pressure (IOP). To demonstrate superiority of IOP control with Istalol 0.5% QD compared to Brimonidine Tartrate 0.2% BID as adjunctive therapy in adults with uncontrolled IOP's (determined by P.I. based on target pressures) currently treated with Latanoprost 0.05% in the study eye(s).

NCT ID: NCT00698438 Completed - Glaucoma Clinical Trials

Comparison Of Trabeculectomy Versus The Ex-PRESS Miniature Glaucoma Device In The Same Patient: A Prospective Randomized Study

XVT-USF
Start date: March 2005
Phase: Phase 4
Study type: Interventional

the purpose of this study was to compare standard trabeculectomy to the Ex-PRESS mini glaucoma shunt implantation under a scleral flap in eyes with open-angle glaucoma.In this report, we describe the results of a prospective, randomized trial in which subjects with bilateral primary open-angle glaucoma underwent the two procedures in fellow eyes.Design: Prospective, randomized clinical trial. Participants: 15 subjects with bilateral primary open-angle glaucoma Methods: Subjects underwent the two procedures in fellow eyes. Safety and efficacy were evaluated for up to two years. Main Outcome Measures: Mean IOP and surgical success rates. Results: Mean IOP was similar in Ex-PRESS and trabeculectomy eyes at all time points except month 9, when Ex-PRESS eyes had lower mean IOP (13.2 mmHg vs 16.5 mmHg, respectively; p=0.025). Percent IOP reduction was also similar at all time points except postoperative day 1, when trabeculectomy eyes were lower (75.5% vs 65.8%, respectively; p=0.003), likely due to a higher rate of early hypotony in trabeculectomy eyes versus Ex-PRESS eyes (47% vs 7%, respectively). Complete (without medications) and qualified (with or without medications) successes were more common at all IOP cut-off values in Ex-PRESS eyes than trabeculectomy eyes at last visit (p=0.015, p=0.015 respectively). Postoperative complications were uncommon in both groups, but trabeculectomy eyes required more postoperative interventions than Ex-PRESS eyes.

NCT ID: NCT00695747 Completed - Glaucoma Clinical Trials

Intraocular Pressure Control Following One Site Versus Two Site Combined Phacoemulsification/IOL And Trabeculectomy

Start date: January 1998
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the safety & effectiveness of the two types of cataract and glaucoma surgeries. Results from this study may improve the surgical and post surgical management and long term management of patients with these conditions in the future

NCT ID: NCT00694876 Completed - Glaucoma Clinical Trials

Impact of Health Literacy and Other Factors on Glaucoma Patient Adherence in South India

Start date: June 2008
Phase: N/A
Study type: Observational

The purpose of this study is to determine how health literacy impacts glaucoma patient adherence (as measured by following up with the doctor) in Tamil Nadu, India. We hypothesize that individuals with better health literacy will have higher rates of follow-up with their ophthalmologist.

NCT ID: NCT00691717 Completed - Open-angle Glaucoma Clinical Trials

Anecortave Acetate Safety in Patients With Open-Angle Glaucoma or Ocular Hypertension

Start date: June 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study was to evaluate the safety and intraocular-lowering efficacy of anecortave acetate depot when administered by anterior juxtascleral depot (AJD) for the treatment of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

NCT ID: NCT00691639 Completed - Open-Angle Glaucoma Clinical Trials

Collection of Blood Specimens From Patients in AL-3789 Studies for Elevated Intraocular Pressure (IOP)

Start date: March 2008
Phase: N/A
Study type: Observational

The objective of this study is to obtain blood samples from patients who are or were participants in any Alcon AL-3789 clinical trial. Association will be conducted to search for genetic markers in patients with glaucoma or ocular hypertension.

NCT ID: NCT00690794 Completed - Ocular Hypertension Clinical Trials

Travatan Z in Ocular Surface Health in Patients With Open-Angle Glaucoma or Ocular Hypertension

Start date: July 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare two ophthalmic solutions in patients with open-angle glaucoma or ocular hypertension.

NCT ID: NCT00683501 Completed - Glaucoma Clinical Trials

Safety, Efficacy, and Pharmacokinetic Profile of DNB-001 in Subjects With Elevated Intraocular Pressure

DNB-001
Start date: October 2007
Phase: Phase 1/Phase 2
Study type: Interventional

A Multi-Centre, Double-Blind, Randomised, Parallel-Group, Placebo-Controlled Phase 1I Study to Investigate the Safety, Efficacy, and Pharmacokinetic Profile of Twice-Daily DNB-001 in Previously Untreated Patients with intraocular Hypertension

NCT ID: NCT00680329 Completed - Ocular Hypertension Clinical Trials

Glaucoma Adherence Study, Spain

GAS
Start date: May 2008
Phase: Phase 4
Study type: Observational

The purpose of this study is to evaluate adherence to DuoTrav® when reinforced by the use of the Travalertâ„¢ Dosing Aid.

NCT ID: NCT00676637 Completed - Ocular Hypertension Clinical Trials

Glaucoma Adherence Study

GAS
Start date: May 2008
Phase: Phase 4
Study type: Observational

The purpose of this study is evaluate adherence to DuoTrav® when reinforced by the use of the Travalertâ„¢ Dosing Aid.