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Keratoconjunctivitis Sicca clinical trials

View clinical trials related to Keratoconjunctivitis Sicca.

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NCT ID: NCT01890941 Completed - Dry Eye Syndromes Clinical Trials

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

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

The purpose of this study is to evaluate the efficacy and safety of KCT-0809 compared to placebo in patients with dry eye syndromes.

NCT ID: NCT01882413 Completed - Dry Eye Syndromes Clinical Trials

A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients Prior to Cataract Removal

REVEAL
Start date: June 2013
Phase: N/A
Study type: Observational

This study will evaluate the prevalence of inflammatory dry eye disease in patients prior to cataract surgery. No treatment is administered in this study.

NCT ID: NCT01864330 Completed - Dry Eye Syndrome Clinical Trials

Influence of Lachrymal Substitutes on Tear Film Thickness in Patients With Moderate Dry Eye Syndrome

Start date: May 2013
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, information about 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 optical coherence tomography (OCT) has become available. The aim of the present study is to assess corneal residence time of three different formulations of topical lubricants, in particular Thealoz Duo® Eye Drops, Hyabak® Eye Drops and Hydrabak® Eye Drops in patients with moderate 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: NCT01863368 Completed - Dry Eye Syndrome Clinical Trials

Clinical Evaluation of Systane® ULTRA Compared to OPTIVE® in Ocular Surface Staining

Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare Systane® ULTRA lubricant eye drops to OPTIVE® lubricating eye drops for ocular surface staining within dry eye subjects and to evaluate the safety of Systane® ULTRA after 3 months of use.

NCT ID: NCT01854905 Completed - Dry Eye Syndromes Clinical Trials

An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusis (LASIK) Therapy

Start date: May 2013
Phase: N/A
Study type: Observational

This is an observational, study of dry eye in patients at the consultation visit prior to LASIK surgery. There is no treatment administered or intervention during the study.

NCT ID: NCT01850979 Completed - Dry Eye Syndrome Clinical Trials

Treatment of Dry Eye Using 0.03% Tacrolimus Eye Drops

Start date: February 2010
Phase: Phase 4
Study type: Interventional

Aqueous deficiency dry eye is mainly caused by Sjogren syndrome (SS), an autoimmune, chronic, inflammatory and systemic disease which affects most commonly the lacrimal and salivary glands.The ocular treatment is focused in increasing lubrification and decreasing inflammation with topical autologous serum, topical immunosuppressive agents and corticotherapy. Use of topical immunosuppressants has increased in recent years because the topical corticotherapy leads to ocular complications. The most used immunosuppressant is cyclosporine. Tacrolimus , another immunosuppressant, has been used in treatment of immune and inflammatory ocular diseases.This study describes a prospective controlled double-blinded randomized study of the clinical outcome of SS dry eyes patients treated with 0.03% tacrolimus eye drops. As secondary purposes, outcome of dry eye symptoms and any ocular symptoms of the eye drops were also questioned to the patients.

NCT ID: NCT01843894 Completed - Dry Eye Clinical Trials

A Phase 1/2, RU-101 Ophthalmic Solution in Patients With Severe Dry Eye

Start date: April 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Objectives: Primary - To determine the safety and tolerability of escalating doses of RU-101 for 4 weeks in patients with severe dry eye Secondary - To explore the efficacy of RU-101 - To explore optimal endpoints for future studies

NCT ID: NCT01840787 Completed - Dry Eye Syndromes Clinical Trials

A Pilot Study on the Use of a Sensory Panel to Assess Comfort Between Three Different Contact Lenses

NAISMITH
Start date: April 2013
Phase: N/A
Study type: Interventional

As new contact lens products continue to be developed and improved, it's becoming harder for some individuals to tell whether one product is different from another. In addition, not everyone has the same level of sensitivity of their eyes, making it difficult for these judgments to be made. The purpose of this study is to explore the idea of using a pre-determined "expert panel" of individuals who are able to tell differences between contact lenses based on their comfort.

NCT ID: NCT01833117 Completed - Dry Eye Clinical Trials

Efficacy and Safety Study of FID 119515A

Start date: May 2013
Phase: N/A
Study type: Interventional

The purpose of this study was to compare the effect of FID 119515A to Blink® Tears on the integrity of tear film in adults with a history of dry eye in both eyes.

NCT ID: NCT01826812 Completed - Dry Eye Syndromes Clinical Trials

Impairment of Reading Ability in Dry Eye Patients

Start date: April 2013
Phase: N/A
Study type: Observational

To assess the reading function impairment in patients with dry eye and to assess the effects of reading on the ocular surface.