Nystagmus Eye Diseases Nystagmus and other irregular eye movements
Conditions
Interventions
Patients will take part in the trial for a total duration of 8 weeks. This will comprise of 2 weeks of spectacle wear followed by 2 weeks of hard or soft contact lens wear. The next 2 weeks the patien
Sponsors
University of Leicester (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Infantile nystagmus over the age of 16 years, either sex
Exclusion criteria
Exclusion criteria: 1. Currently involved in surgical or pharmacological trials for the treatment of nystagmus 2. Previous corneal trauma or intolerence to contact lens wearing
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in nysatgmus intensity measured with eye movement recordings, measured at baseline, day 14, day 28, day 42 and day 56. | — |
Secondary
| Measure | Time frame |
|---|---|
| Measured at baseline, day 14, day 28, day 42 and day 56: 1. Changes in LogMAR (chart) visual acuity at 4M (with head free) 2. Changes in LogMAR (chart) visual acuity at 0.4M (with head free) 3. Change in gaze dependant visual acuity at 4M 4. Change in nystgamus intensity, NAFX function and reading speed will be evaluated from the eye movement recordings at different fixation points across the horizontal plane 5. Subjective changes in visual function evaluated with the VFQ25 | — |
Countries
United Kingdom
Outcome results
None listed