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Dry Eye Syndromes clinical trials

View clinical trials related to Dry Eye Syndromes.

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NCT ID: NCT01441895 Recruiting - Cataract Clinical Trials

Corneal Sensation and Incidence of Dry Eye Post Refractive Cataract Extraction With FemtoSecond Laser

Start date: September 2011
Phase: N/A
Study type: Observational

The study objective is to assess changes in corneal sensation and dry eye signs and symptoms following cataract extraction/femtosecond arcuate relaxing incisions. Our clinical hypothesis is to determine if a combination of cataract surgery and femtosecond arcuate relaxing incisions lead to a reduction in corneal sensation and the onset or worsening of dry eye signs and symptoms.

NCT ID: NCT01434277 Completed - Dry Eye Syndromes Clinical Trials

Safety Evaluation of a New Preservative in a Lubricating Eye Drop

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

This study is to evaluate the safety of a new preservative in a lubricant eye drop used four times a day in healthy adults and subjects diagnosed with dry eye.

NCT ID: NCT01427816 Completed - Dry Eye Syndromes Clinical Trials

A Phase II Study of KCT-0809 in Patients With Dry Eye Syndrome

Start date: n/a
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of KCT-0809 compared to placebo in patients with dry eye syndrome.

NCT ID: NCT01421498 Completed - Dry Eye Disease Clinical Trials

Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OPUS-1)

OPUS-1
Start date: August 29, 2011
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the efficacy of SAR 1118 Ophthalmic Solution (5.0%) compared to placebo in the treatment of Dry Eye. The safety and tolerability of SAR 1118 Ophthalmic Solution (5.0%) compared to placebo in subjects with dry eye when administered BID for 12 weeks will also be evaluated.

NCT ID: NCT01393132 Completed - Dry Eye Clinical Trials

Comparative Study of Thymosin Beta 4 Eye Drops vs. Vehicle in the Treatment of Severe Dry Eye

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

Severe dry eye is a debilitating ocular disease resulting in loss of vision, reduced day-to-day function and significant discomfort. Tear substitutes are an important part of the treatment of all patients, however, even with aggressive us, the corneal(ocular)surface often remains very irregular due to poor surface healing. The agent being evaluated in this study, Thymosin Beta 4, promotes healing of the corneal surface and has been studied in patients with recalcitrant corneal ulcers and erosions with significant success (Arch Ophthalmol. 2010;128(5):636-638., Ann of the NY Acad of Sci, May, 2010). The study hypothesis is that Thymosin Beta 4, in its role as a modulator of corneal surface healing, may be able to promote healing of the corneal surface allowing for more conventional modalities to take over and maintain a smooth and regular ocular surface. The investigators hope to be able to demonstrate an improvement in visual acuity, surface healing and a reduction in dry-eye related symptoms.

NCT ID: NCT01388426 Completed - Dry Eye Clinical Trials

Moisture Chamber Glasses for Dry Eye in Asian Population

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

Objective of this study is to evaluate the tolerance and potential benefit of moisture chamber glasses for dry eye in an Asian population. In this clinic based prospective interventional study, we aim to recruit patients (until 10 patients complete the study) who have evaporative dry eye due to exposure to environmental stress (such as frequency of out door activities) and keen to try out moisture chamber glasses/ eyewear from the dry eye clinic in Singapore National Centre. After informed consent, these patients will be prescribed 7eye( Panoptx)™ moisture chamber glasses/eyewear for 3 months and will be monitored on a diary for the amount of time wearing eyewear for 2 weeks and the number of eye drops for each type of medication used. Other outcomes will be changes in symptoms of dry eye using visual analog scale, as well as objective signs of dry eye (eg. corneal fluorescence staining and tear break up time (TBUT). As moisture chamber spectacles are currently not available as a treatment option for dry eye in Singapore, the findings of this study will give an insight to the efficacy of this new treatment modality in our population.

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: NCT01386073 Recruiting - Dry Eye Clinical Trials

Efficacy of FreshKote and Systane for the Treatment of Dry Eye and Improvement of Osmolarity

Start date: July 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy of FreshKote and Systane for the reduction of dry eye signs and symptoms.

NCT ID: NCT01382810 Recruiting - Dry Eye Syndromes Clinical Trials

Altaire Gel Forming Solution Versus Refresh Tears for the Treatment of Dry Eye Signs and Symptoms

Start date: March 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate and compare the effects of Altaire Gel forming solution and Refresh Tears in mild-moderate dry eye patients.

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.