Treatment Trials

3 Clinical Trials for Various Conditions

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      COMPLETED
      Corneal Staining and Physiological Compromise After Eight Hours of Soft Contact Lens Wear
      Description

      The purpose of this study is to assess corneal staining and to measure the relative corneal epithelial "barrier" function (the degree to which the cornea can prevent penetration of colored sodium fluorescein dye into the eye) after 8 hours of wear with a known soft contact lens and multipurpose lens care solution combination.

      Conditions
      Contact Lens-induced Corneal Fluorescein Staining
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      COMPLETED
      Prolongation of Contact Lens Comfortable Wear Duration by CLM2 Topical Gel
      Description

      This study compares contact lens comfortable wear duration, and signs and symptoms of contact lens discomfort, test versus control.

      Conditions
      Contact Lens DiscomfortContact Lens-induced Corneal DisorderContact Lens Acute Red EyeContact Lens-induced Corneal Fluorescein Staining
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      COMPLETED
      Soft Contacts Observation of Risk and Education (SCORE)
      Description

      Specific Aims 1. Develop risk assessment scores for SCL wearers 2. Test the scoring algorithm in SCL wearers who present with adverse events 3. Explore targeted patient education to reduce risk behaviors associated with SCL wear.

      Conditions
      Contact Lens ComplicationContact Lens Acute Red EyeContact Lens Related Corneal Infiltrate (Disorder)Contact Lens-Induced Corneal Fluorescein Staining
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