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Clinical Trials/NCT00816569
NCT00816569UnknownNot Applicable

Orthokeratology Contact Lenses for Keratoconus

Hadassah Medical Organization2 sites in 1 country30 target enrollmentStarted: February 2009Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
30
Locations
2
Primary Endpoint
Uncorrected Visual acuity

Study Overview

Brief Summary

To investigate a possible benefit of Orthokeratology contact lenses to improve uncorrected visual acuity of keratoconus patients

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Moderate Keratoconus
  • No apical scars

Exclusion Criteria

  • Advanced Keratoconus
  • Apical scaring
  • Contact lens intolerance

Outcomes

Primary Outcomes

Uncorrected Visual acuity

Time Frame: After 1 month

Secondary Outcomes

  • Amount of change in corneal video-topography(At one month)

Investigators

Sponsor Class
Other

Study Sites (2)

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