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A Comparison of Fellow Eyes Undergoing LASIK or PRK With a Wavefront-guided Excimer Laser Versus a Wavefront-optimized Excimer Laser

E

Edward E. Manche

Status

Completed

Conditions

Myopia
Astigmatism
Hyperopia

Treatments

Procedure: LASIK and PRK

Study type

Interventional

Funder types

Other

Identifiers

NCT01135719
SU-04302009-2458

Details and patient eligibility

About

Subjects with myopia, hyperopia and astigmatism are being randomized to be treated in one eye with a wavefront-guided excimer laser and their fellow eye treated with a wavefront-optimized excimer laser.

Full description

Subjects with myopia, hyperopia and astigmatism are being randomized by ocular dominance to be treated with either PRK or LASIK. One eye will be treated with a wavefront-guided excimer laser and the fellow eye will be treated with a wavefront optimized excimer laser.

Enrollment

137 patients

Sex

All

Ages

21 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Healthy subjects age 21 and older.
  • Subjects with nearsightedness, farsightedness and/or astigmatism.

Exclusion Criteria:Autoimmune diseases.

  • Children.
  • Women pregnant or nursing.
  • Ectatic corneal disease.
  • Previous ocular surgery.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

137 participants in 2 patient groups

Wavefront guided LASIK/PRK
Active Comparator group
Description:
Wavefront-guided LASIK/PRK
Treatment:
Procedure: LASIK and PRK
Wavefront optimized LASIK/PRK
Active Comparator group
Description:
Wavefornt optimized LASIK/PRK
Treatment:
Procedure: LASIK and PRK

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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