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Dry Eye Syndromes clinical trials

View clinical trials related to Dry Eye Syndromes.

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NCT ID: NCT02597803 Completed - Dry Eye Syndrome Clinical Trials

Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-1

Start date: September 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The objective of this study is to compare the safety and efficacy of RGN-259 Ophthalmic Solutions to placebo for the treatment of the signs and symptoms of dry eye.

NCT ID: NCT02585648 Completed - Dry Eye Syndromes Clinical Trials

Added Benefits of Lachrymal Substitute Gel During the Night in Patients With Moderate to Severe Dry Eye Syndrome

Start date: February 2016
Phase: N/A
Study type: Interventional

Dry eye syndrome is a highly prevalent ocular disease with an increasing incidence in the elderly population. Topically administered lubricants are the basis for treatment of this disease. Relief of symptoms in patients with moderate to severe dry eye disease is usually reached by the use of artificial tears during the day. Nighttime relief is often achieved by substances known to be more adhesive to the ocular surface, such as gels.

NCT ID: NCT02585453 Completed - Dry Eye Syndromes Clinical Trials

Influence of Lachrymal Substitute Gels on Tear Film Thickness in Patients With Moderate to Severe Dry Eye Syndrome

Start date: April 2015
Phase: Phase 4
Study type: Interventional

Dry eye syndrome is a highly prevalent ocular disease with an increasing incidence in the elderly population. Topically administered lubricants are the basis for treatment of this disease. However, exact information about the tear film thickness and the corneal residence time of topical lubricants is still sparse, therefore no ideal treatment regimen has been found. Recently a new method for assessment of tear film thickness based on ultra high resolution optical coherence tomography (OCT) has become available. The aim of the present study is to assess tear film thickness and corneal residence time of three different formulations of topical lubricants, in particular Thealoz Duo® Eye Drops, Hylo® Gel Eye Drops and Systane® Gel Eye Drops in patients with moderate to severe dry eye disease. In addition, standard tests for dry eye syndrome, such as the ocular surface disease index (OSDI©), Schirmer I test and determination of tear break up time (BUT) will be performed.

NCT ID: NCT02554981 Completed - Dry Eye Syndromes Clinical Trials

Evaluation of Maintaining Visual Performance in Participants Who Engage in Electronic Visual Tasking While Using Restasis®

EMPOWER
Start date: July 21, 2015
Phase: Phase 4
Study type: Interventional

This study will evaluate the efficacy of Restasis® in participants with dry eye disease who engage in electronic visual tasking.

NCT ID: NCT02553772 Completed - Dry Eye Syndromes Clinical Trials

A Safety and Efficacy Study of a New Eye Drop Formulation in Patients With Dry Eye Disease.

Start date: January 6, 2016
Phase: Phase 3
Study type: Interventional

This study will evaluate the safety and efficacy of a new eye drop formulation in patients with dry eye disease.

NCT ID: NCT02526290 Completed - Dry Eye Syndromes Clinical Trials

Six Month Study to Evaluate the Safety and Effectiveness of the Intranasal Lacrimal Neurostimulator

Start date: August 31, 2015
Phase: N/A
Study type: Interventional

In this study, the safety and effectiveness of the Oculeve Intranasal Lacrimal Neurostimulator after 180 days of use in participants with aqueous tear deficiency will be evaluated.

NCT ID: NCT02522312 Completed - Dry Eye Syndrome Clinical Trials

A Retrospective Analysis of Restasis® Benefits in Dry Eye Contact Lens Patients

Start date: September 2015
Phase: N/A
Study type: Observational

A retrospective analysis of Restasis® benefits in dry eye contact lens patients.

NCT ID: NCT02510235 Completed - Dry Eye Syndrome Clinical Trials

Tolerability, Safety and Efficacy of Lubricin Eye Drops vs Sodium Hyaluronate Eye Drops in Subjects With Mod. Dry Eye

Start date: March 2015
Phase: N/A
Study type: Interventional

Dry eye is a multifactorial disease of the tears and ocular surface that results in symptoms of discomfort, visual disturbance, and tear film instability with potential damage to the ocular surface. It is accompanied by increased osmolarity of the tear film and inflammation of the ocular surface. Lubricin is a mucin-like glycoprotein originally discovered in synovial fluid, as a secreted product of cells that line the joint tissues, which is present at the surface of articular cartilage and it has been investigated on its roles at the ocular surface, in normal and pathologic conditions such as dry eye. The objective of the study is to assess the tolerability, safety and efficacy of Lubricin eye drops solution administered over 4 weeks versus sodium hyaluronate (Na-HY) eye drops solution in subjects with moderate dry eye.

NCT ID: NCT02507934 Completed - Dry Eye Syndrome Clinical Trials

Tolerability, Safety and Efficacy of Lubricin (150 µg/ml) Eye Drops Versus Sodium Hyaluronate (HA) 0.18% Eye Drops in Patients With Moderate Dry Eye (DE)

Start date: June 2015
Phase: N/A
Study type: Interventional

Dry eye is a multifactorial disease of the tears and ocular surface that results in symptoms of discomfort, visual disturbance, and tear film instability with potential damage to the ocular surface. It is accompanied by increased osmolarity of the tear film and inflammation of the ocular surface. Lubricin is a mucin-like glycoprotein originally discovered in synovial fluid, as a secreted product of cells that line the joint tissues, which is present at the surface of articular cartilage and it has been investigated on its roles at the ocular surface, in normal and pathologic conditions such as dry eye. The objective of the study is to assess the tolerability, safety and efficacy of Lubricin eye drops solution administered over 4 weeks versus sodium hyaluronate (Na-HY) eye drops solution in subjects with moderate dry eye.

NCT ID: NCT02503189 Completed - Clinical trials for Dry Eye With Sjögren's Syndrome

A Phase III Study of KCT-0809 in Dry Eye Patients With Sjögren's Syndrome

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the superiority of KCT-0809 to placebo, and to evaluate safety in dry eye patients with Sjögren's syndrome