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Keratoconjunctivitis Sicca clinical trials

View clinical trials related to Keratoconjunctivitis Sicca.

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NCT ID: NCT00201981 Completed - Clinical trials for Keratoconjunctivitis Sicca

Study of Rebamipide Eye Drops to Treat Dry Eye

Start date: May 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the potential safety and effectiveness of rebamipide eye drops, an investigational eye drop being developed for the treatment of keratoconjunctivitis sicca (dry eye).

NCT ID: NCT00201955 Completed - Clinical trials for Keratoconjunctivitis Sicca

Study of Rebamipide Eye Drops to Treat Dry Eye

Start date: May 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the potential safety and effectiveness of rebamipide eye drops, an investigational eye drop being developed for the treatment of keratoconjunctivitis sicca (dry eye).

NCT ID: NCT00198536 Completed - Dry Eye Syndromes Clinical Trials

Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome

Start date: April 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether ecabet ophthalmic solution is an effective treatment for dry eye syndrome

NCT ID: NCT00128245 Completed - Clinical trials for Keratoconjunctivitis Sicca

Safety and Efficacy of Pimecrolimus Ophthalmic Suspension in Patients With Moderate to Severe Keratoconjunctivitis Sicca

Start date: September 2004
Phase: Phase 2
Study type: Interventional

This study evaluates the efficacy and safety of 2 doses of pimecrolimus (0.3% and 1%) ophthalmic suspension in a moderate to severe population of keratoconjunctivitis sicca (KCS, dry eye syndrome) patients.

NCT ID: NCT00037661 Completed - Clinical trials for Keratoconjunctivitis Sicca

Study of INS365 Ophthalmic Solution in a Controlled Adverse Environment in Patients With Dry Eye

Start date: April 2002
Phase: Phase 3
Study type: Interventional

Comparative efficacy trial of INS365 Ophthalmic Solution and placebo in patients with dry eye.

NCT ID: NCT00025818 Completed - Clinical trials for Arthritis, Rheumatoid

Six Month Clinical Research Study for Patients With Moderate or Severe Dry Eye Syndrome

Start date: May 2001
Phase: Phase 3
Study type: Interventional

A six-month clinical research trial to evaluate the effectiveness of an investigational medication for the treatment of dry eye syndrome in patients that have been diagnosed with moderate to severe dry eye syndrome, an autoimmune disorder AND/OR females 65 years of age or older.

NCT ID: NCT00001731 Completed - Sjogren's Syndrome Clinical Trials

Treatment of Dry Eye Syndrome With Cyclosporin A Eye Drops

Start date: November 1997
Phase: Phase 2
Study type: Interventional

This study will examine whether cyclosporin A eye drops alleviate dry eye syndrome, a disorder of tear deficiency or excessive tear evaporation. The condition damages the surface of the eye and causes discomfort. Age-related dry eye syndrome may result from a problem with the immune system in which cells called lymphocytes infiltrate the tear glands and cause a chronic, progressive inflammatory process. Previous studies suggest that cyclosporin A may increase tear production or decrease inflammation on the surface of the eye, or both, improving dry eye symptoms. Patients in the study will undergo a complete eye examination, and a small tear sample will be collected to study tear consistency and composition. A small amount of conjunctiva (the clear, thin covering of the eye lining the eyelids and eyeball) will be removed to study substances in it that might provide information on what causes dry eye. A blood sample also will be taken to look for antibodies found in patients with Sjogren's syndrome, a disorder characterized by dryness of the mouth, eyes and other mucous membranes. Patients will also fill out forms providing information on the extent to which their dry eyes bother them. Patients will be randomly divided into two treatment groups: one will take a cyclosporin 0.1% eye drop emulsion; the other will take the emulsion vehicle alone-that is, the same drops but without the active ingredient cyclosporin. Both groups will take one drop in each eye 4 times a day for 2 months. Neither the patients nor the doctors will know which patients are receiving which medication until the study ends. All patients will also be given artificial teardrops to use for comfort if needed.