Status:
COMPLETED
Patient Satisfaction in Post-LASIK Patients With Presbyopia-Correcting IOLs vs. Post-Lasik Patients With Monofocal IOLs
Lead Sponsor:
Bucci Laser Vision Institute
Conditions:
Patient Satisfaction
Eligibility:
All Genders
Brief Summary
Compare functional visual outcomes and patient satisfaction of post-LASIK patients having received presbyopia-correcting IOLs versus post-LASIK patients having received monofocal IOLs
Eligibility Criteria
Inclusion
- Post-LASIK
- Post cataract surgery
- Implantation of ZLB00, ZXR or ZXT, ZCB00, or AO60 intraocular lenses
- Spherical values greater than ± 0.50 and/or cylinder magnitude greater than 0.75D
Exclusion
- Any vision-limiting problems (e.g., corneal, retinal, infection) which could potentially limit their post-operative visual potential
- Any newly acquired ocular condition or pathology (e.g., ARMD, epiretinal membrane, chronic dry eye, irregular astigmatism, diabetic retinopathy)
- Max sphere no greater than ± 0.50D and cylinder less than and/or equal to 0.75D
Key Trial Info
Start Date :
October 25 2019
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2020
Estimated Enrollment :
44 Patients enrolled
Trial Details
Trial ID
NCT04134507
Start Date
October 25 2019
End Date
December 1 2020
Last Update
December 17 2020
Active Locations (1)
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1
Bucci Laser Vision
Wilkes-Barre, Pennsylvania, United States, 18702