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Dry Eye clinical trials

View clinical trials related to Dry Eye.

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NCT ID: NCT02701764 Completed - Dry Eye Clinical Trials

Can Pregabalin Reduce the Frequency and Severity of Dry Eye Symptoms After Laser-assisted in Situ Keratomileusis?

Start date: July 26, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Can Lyrica (Pregabalin) help prevent severe Dry Eye post LASIK surgery?

NCT ID: NCT02511379 Terminated - Dry Eye Clinical Trials

Clinical Evaluation of Systane® Balance in Dry Eye Subjects

Start date: November 26, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Systane® Balance following 90 days of QID (4 times/day) dosing among Indian subjects with dry eye.

NCT ID: NCT02493244 Completed - Dry Eye Clinical Trials

Lipid Layer Thickness Pre and Post Lid Scrubs With Cliradex

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

Tears play a vital role in vision. A thin layer of tears is always present to cover the surface of the eye for optimal comfort and vision. There are several layers to the tear film, and the outer most layer is comprised of lipids. This lipid layer prevents evaporation of the tears and may be disrupted in people suffering from symptoms of dry eye. Cleaning eyelids with Cliradex wipes have shown to be effective in reducing dry eye symptoms in some patients, and the purpose of this study is to evaluate the tear film lipid layer thickness before and after one months treatment with Cliradex Wipes.

NCT ID: NCT02481167 Recruiting - Dry Eye Clinical Trials

Evaluation of Meibomian Gland Dysfunction in Chinese Old Patients

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

The purpose of this study is to identify age-related changes in chinese meibomian glands that may be associated with meibomian gland dysfunction (MGD).

NCT ID: NCT02470429 Completed - Dry Eye Clinical Trials

Evaluation of Clinical Outcomes After the Use of SYSTANE® HYDRATION

Start date: July 17, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare SYSTANE® HYDRATION to Hyabak 0.15% based on total ocular surface staining scores (TOSS) at Day 42.

NCT ID: NCT02468700 Completed - Dry Eye Clinical Trials

OTX-14-006: A Phase 2 Study Evaluating the Safety and Efficacy of OTX-DP for the Treatment of Dry Eye

Start date: January 2015
Phase: Phase 2
Study type: Interventional

The objective of the study was to evaluate the efficacy and safety of OTX-DP (dexamethasone insert) 0.4 mg for intracanalicular use when placed in the canaliculus of the eyelid for the treatment of the signs and symptoms of dry eye disease

NCT ID: NCT02420834 Completed - Dry Eye Clinical Trials

Dry Eye Treatment With Artificial Tears

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

Dry eye is a chronic irritating eye condition that affects many people, caused by poor tear quality and insufficient quantity. Treatments are traditionally in the form of artificial tears applied to the ocular surface. However, there is little evidence in the scientific literature that demonstrates their efficacy relative compared to each other, nor how to decide which one might be most effective for an individual patient. Therefore the investigators aim to examine the efficacy of different classes of artificial tears (those designed to increase viscosity, reduce evaporation or to mimic the component balance of the natural tears). In addition, the investigators also aim to determine how the treatment preferred by an individual could potentially have been predicted from their baseline condition.

NCT ID: NCT02417116 Completed - Dry Eye Clinical Trials

Tear Osmolarity Clinical Utility in Dry Eye Disease

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

Millions of people suffer from dry eye disease, causing symptoms such as redness, burning, feeling of sand or grit in the eye and light sensitivity. Dry eye disease occurs when your eyes do not produce enough tears or produce poor quality tears. This can happen for a number of reasons, including aging, hormonal changes in women and side effects of diseases or medications. It is now possible to objectively measure the degree of dry eye disease by collecting a tiny sample of tears from the corner of the eye and then measuring the amount of salt in the tears (termed osmolarity). We aim to establish the overall levels of raised and normal tear osmolarity in people presenting to the eye clinic with complaints of dry eye, and relate this to other factors such as symptoms, topical and nutritional medication and dry eye treatment.

NCT ID: NCT02405039 Active, not recruiting - Dry Eye Clinical Trials

Study of EBI-005 in Dry Eye Disease (DED)

EBI-005
Start date: April 2015
Phase: Phase 3
Study type: Interventional

This is a randomized, double masked study designed to evaluate the safety of EBI-005 5 mg/mL topical ophthalmic solution given three times daily (TID) compared to vehicle-control over a one year period in subjects with dry eye disease (DED). Approximately 188 subjects will be enrolled to either EBI-005 or vehicle at up to 15 centers in the United States (US) and Canada.

NCT ID: NCT02380248 Completed - Dry Eye Clinical Trials

Clinical Evaluation of Systane® Gel Drops in Dry Eye Subjects

Start date: May 14, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Systane® Gel Drops in dry eye subjects following 90 days of QID (4 times/day) dosing.