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Dry Eye Syndrome clinical trials

View clinical trials related to Dry Eye Syndrome.

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NCT ID: NCT01675570 Completed - Dry Eye Syndrome Clinical Trials

A Study of RX-10045 in the Treatment of Dry Eye Disease

Start date: August 2012
Phase: Phase 2
Study type: Interventional

The primary purpose of this study is to assess the efficacy, tolerability and safety of RX-10045 Ophthalmic Solution in patients with Dry Eye Disease.

NCT ID: NCT01670357 Completed - Dry Eye Syndrome Clinical Trials

Phase II Study of DA-6034 Eye Drops in Dry Eye Syndrome

DES
Start date: April 2012
Phase: Phase 2
Study type: Interventional

This study is to determine the efficacy and safety of 3% or 5% DA-6034 eye drops compared with placebo in dry eye syndrome.

NCT ID: NCT01632137 Completed - Dry Eye Syndrome Clinical Trials

Efficacy and Safety of Rebamipide in Subjects With Dry Eye Syndrome

Start date: June 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of rebamipide ophthalmic suspension in subjects with dry eye syndrome.

NCT ID: NCT01614600 Completed - Myopia Clinical Trials

Clinical Evaluation of a Daily Disposable Contact Lens in Symptomatic Weekly/Monthly Lens Wearers

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the reduction of contact lens-related dryness symptoms when symptomatic weekly/monthly contact lens wearers were switched to DAILIES® AquaComfort Plus® lenses for a two-week period using composite scores on the Contact Lens Dry Eye Questionnaire (CLDEQ).

NCT ID: NCT01579539 Completed - Dry Eye Syndrome Clinical Trials

The Effect of Intravenous Glucocorticoids on the Tearfilm in Eyes With Thyroid-associated Ophthalmopathy

Start date: June 27, 2013
Phase: Phase 3
Study type: Interventional

Thyroid-associated ophthalmopathy (TAO), also called Graves' ophthalmopathy or thyroid eye disease, is a common orbital disease in adults. Patients with TAO, especially in its active phase, often complain about symptoms of ocular surface discomfort, including excess tearing, gritty sensation, increased sensitivity to light and foreign-body sensation, which are similar to inflammatory ocular surface disorders such as dry-eye syndrome (DES). Incomplete blink, increased proptosis and greater palpebral fissure width in TAO accelerates tear evaporation, which increases the tear fluid's osmolarity, and results in ocular surface damage. The administration of intravenous glucocorticoids can be an effective treatment for TAO. The rationale of the present study is to assess the effect of intravenously administered glucocorticoids on the signs of DES in patients with TAO with new methods such as measurement of tear film thickness, tear film osmolarity and scattering of the tear film and well established methods for assessment of the severity of DES. Additionally, impression cytology and determination of tear cytokines/chemokines will be performed to obtain information about inflammatory processes on the ocular surface.

NCT ID: NCT01541891 Completed - Dry Eye Syndrome Clinical Trials

Efficacy and Safety of PRO-148 Ophthalmic Solution Versus SYSTANE® in the Treatment of Patients With Dry Eye Syndrome

PRO-148
Start date: October 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of PRO-148 ophthalmic solution compared with SYSTANE ® ophthalmic solution for the treatment of signs and symptoms of mild-to-moderate dry eye syndrome.

NCT ID: NCT01483989 Completed - Dry Eye Syndrome Clinical Trials

In Vivo Measurement of Corneal Epithelial Changes in Dry Eye Patients

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to measure corneal epithelial changes in dry eye subjects using a novel lubricant eye gel.

NCT ID: NCT01387347 Completed - Dry Eye Clinical Trials

Safety and Efficacy of Thymosin Beta 4 Ophthalmic Solution in Patients With Dry Eye

Start date: August 2011
Phase: Phase 2
Study type: Interventional

Thymosin Beta 4 (Tβ4) is a synthetic copy of the naturally-occurring 43-amino acid peptide that is found in a variety of tissues. Tβ4 promotes/accelerates wound repair in dermal, ocular, and cardiac animal models. Two recent pre-clinical evaluations have demonstrated that Tβ4 promotes corneal ocular surface defects healing in animal models of dry eye. RGN-259 (formulation of Tβ4 ophthalmic solution) mechanism of action offers potential to be a product that meets a major unmet medical need in patients with dry eye.

NCT ID: NCT01382225 Completed - Dry Eye Syndrome Clinical Trials

Sodium Hyaluronate Ophthalmic Solution, 0.18% for Treatment of Dry Eye Syndrome

Start date: July 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine if Sodium Hyaluronate, 0.18% is effective in treating the signs and symptoms of dry eye disease.

NCT ID: NCT01339936 Completed - Dry Eye Syndrome Clinical Trials

Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of an Investigational Eye Drop in Dry Eye Sufferers

Start date: March 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The main objectives of the investigation will be to assess the effect of the repeated usage of an investigational eye drop on the tear film characteristics of dry eye sufferers and demonstrate the benefit of this eye drops for dry eye sufferers.