Status:
COMPLETED
Evaluation of Outcomes Following LASIK Surgery Using CustomVue
Lead Sponsor:
Medical University of South Carolina
Conditions:
Myopia
Astigmatism
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of the study was to evaluate visual outcomes, contrast sensitivity, glare and induced high order aberrations induced by the new CustomVue software use for wavefront-guided LASIK.
Eligibility Criteria
Inclusion
- Myopia 0.00 to -6.00 D
- Astigmatism 0.00 up to -3.00 D
- Manifest refraction spherical equivalent (MRSE) up to -6.00 D.
Exclusion
- History of ocular pathology
- Previous ocular surgery
- Large pupils (greater than 8mm diameter, infrared measurement)
- Thin corneas (preoperatively calculated minimal residual bed \< 250 um)
- Irregular astigmatism
- Asymmetric astigmatism
- Unstable refraction
- Any other condition that precludes the patient from undergoing LASIK
Key Trial Info
Start Date :
September 1 2005
Trial Type :
INTERVENTIONAL
End Date :
February 1 2006
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00366769
Start Date
September 1 2005
End Date
February 1 2006
Last Update
August 21 2006
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.