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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00365677
Other study ID # 441
Secondary ID
Status Completed
Phase N/A
First received June 30, 2006
Last updated December 7, 2011
Start date October 2005
Est. completion date March 2006

Study information

Verified date December 2011
Source Bausch & Lomb Incorporated
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The objective of this study was to compare the safety and effectiveness of two versions of the Bausch & Lomb Zyoptix Tissue Saving Aspheric Algorithm versus the current Zyoptix Tissue Saving Algorithm when used for myopia and myopic astigmatism LASIK treatment.


Recruitment information / eligibility

Status Completed
Enrollment 127
Est. completion date March 2006
Est. primary completion date March 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Myopia with or without astigmatism.

- Normal Corneal topography

- Willing to have both eyes treated with the laser.

Exclusion Criteria:

- Contraindications to LASIK.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
The Bausch & Lomb Zyoptix Tissue Saving Aspheric algorithm
Used with LASIK treatment for the correction of myopia and myopic astigmatism.
The Bausch & Lomb Zyoptix Tissue Saving algorithm
Used with LASIK treatment for the correction of myopia and myopic astigmatism.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bausch & Lomb Incorporated

Outcome

Type Measure Description Time frame Safety issue
Primary Uncorrected visual acuity At 90 days post surgery No
Primary Preservation of best spectacle corrected high contrast logMAR distance visual acuity compared to baseline. At 90 days post surgery No
Secondary Deviation from target correction At 90 days post surgery No
Secondary Improvement in uncorrected distance high contrast logMAR visual acuity compared to baseline At 90 days post surgery No
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