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Optical treatment of nystagmus

A quantitative study comparing hard and soft contact lenses to spectacles on changes in nystagmus oscillations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN80219391
Enrollment
28
Registered
2010-08-11
Start date
2010-09-01
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nystagmus Eye Diseases Nystagmus and other irregular eye movements

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)
Lead Sponsor

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

MeasureTime frame
Changes in nysatgmus intensity measured with eye movement recordings, measured at baseline, day 14, day 28, day 42 and day 56.

Secondary

MeasureTime 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

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026