Dry Eye Syndrome Clinical Trial
Official title:
Eight Week Feasibility Study Enrolling Dry Eye Subjects Confirmed by Four of Seven Dianostic Markers Responding to Nutritional Therapy
Dry eye disease (DED) is a common but often inadequately treated disease of the tears and surface of the eye. It can cause poor vision and chronic pain and is more frequent with increasing age. The 1995 Report of the National Eye Institute/Industry Workshop on Clinical Trials in Dry Eye defined dry eye as "a disorder of the tear film due to tear deficiency or excessive evaporation, which causes damage to the interpalpebral ocular surface and is associated with symptoms of ocular discomfort". The International Dry Eye Work Shop (DEWS) committee subsequently defined dry eye as "a multi-factorial disease of the tears and ocular surface that results in symptoms of discomfort, visual disturbance, and tear film instability with potential damage to the ocular surface. It is accompanied by increased osmolarity of the tear film and inflammation of the ocular surface." Typically, symptoms associated with dry eye disease include ocular burning, foreign body sensation (sand or grit), photophobia (light sensitivity), and other symptoms that result in overall long term discomfort in patients. The proposed eight week feasibility study if dry eye subjects confirmed elevated osmolarity and symptoms respond to nutritional therapy.
Hyperosmolarity is a major cause of cell damage over time and can result in apoptosis of
corneal and conjunctival cells. Determining if a patient has hyperosmolarity is critical
allowing us to offer therapies to correct the problem. Reducing and regulating osmolarity is
important in preventing potential long-term tissue compromise. Treatment leading to
decreasing tear osmolarity can improve the patient's quality of life by stabilizing vision
and, in many cases, simply allowing patients to return to normal activities.
Fatty Acids (EFA) have been shown to diminish inflammatory responses in many human
inflammatory diseases, and interest in the use of omega-3 and omega-6 fatty acids for
disease treatment has resulted in several small studies as well as the use (and
over-the-counter availability) of EFA-containing nutritional supplements, including several
specifically for the treatment of DED. Unfortunately, the effects of Omega 3 on dry eye
disease have not been established to date. The purpose of this study is to better understand
the role of Omega 3 plays in the regulating tear osmolarity in patients with established
findings consistent with dry eye disease.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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