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Patient Reported Satisfaction With Contoura LASIK Utilizing the Phorcides Analytic Software

Myopia Clinical Trial

Official title:
Patient Reported Satisfaction With Contoura LASIK Utilizing the Phorcides Analytic Software

Clinical Trial Summary

The objective is to determine the percentage of subjects satisfied (Completely Satisfied or Very Satisfied) with vision after Phorcides Planned Contoura LASIK.

Clinical Trial Description

This study is a single site, single-arm, prospective, observational study of subject satisfaction, after successful bilateral LASIK surgery. Subjects will be assessed pre-operatively, operatively and at 1 week, 1 month, and 3 months post-operatively. Clinical evaluations will include measurement of visual acuity, manifest refraction, and topography, aberrometry, and administration of the OSDI and PROWL questionnaires. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05848817
Study type Observational
Source Mann Eye Institute
Contact Melissa Hamann Wright
Phone 713-580-2500
Email Melissa.Wright@manneye.com
Status Recruiting
Phase
Start date May 19, 2023
Completion date May 15, 2024
View Details
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