Status | Study |
Completed |
Study Name: Effects of Sevoflurane and Propofol on Light Flashed Evoked Pupillometry Condition: Blindness Date: 2009-04-01 Interventions: Drug: propofol Propofol infusi |
Completed |
Study Name: Determine the Effect of Intraocular Pressure (IOP), Optic Nerve Imaging, Venous Congestion in Volunteers Prone Position 5 Hours Condition: Blindness Date: 2009-04-01 |
Completed |
Study Name: Wayfinding Information Access System for People With Vision Loss Condition: Blindness Date: 2009-01-22 Interventions: Device: Wayfinding Prototype A Wayfinding Prototype is used by subjects to determine any advantages over |
Completed |
Study Name: Blind Child Melatonin Treatment Study Condition: Blindness Date: 2008-06-03 Interventions: Dietary Supplement: Melatonin |
Completed |
Study Name: Blind Elderly Melatonin Treatment Study Condition: Blindness Date: 2008-05-30 Interventions: Biological: Melatonin 0.025 mg |
Completed |
Study Name: Young Blind Child Melatonin Treatment Study Condition: Blindness Date: 2008-05-30 Interventions: Biological: Melatonin 0.1-3 mg, daily, up to 1 year (minimum duration of 6 weeks) |
Completed |
Study Name: Blind Adult Melatonin Treatment Study Condition: Blindness Date: 2008-05-28 Interventions: Drug: Melatonin Dose range: 0.01 mg - 20 mg, daily, up to 5 years (based on each subject's circadian rhy |
Terminated |
Study Name: Unilateral Blindness/ Unilateral Deafness-relation to Neck Pain Condition: Neck Pain Unilateral Blindness Date: 2007-12-23 |
Completed |
Study Name: Treatment of Congenital Stationary Night Blindness With an Alga Containing High Dose of Beta Carotene Condition: Night Blindness Date: 2007-12-05 Interventions: Dietary Supplement: alga Dunaliella bardawil Each patients |
Completed |
Study Name: Do Blue-Blocking Lenses Block Blue Colour From Our Lives? Condition: Blindness Date: 2006-11-22 Interventions: Procedure: cataract surgery |