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Patient Satisfaction in Post-LASIK Patients With Presbyopia-Correcting IOLs vs. Post-Lasik Patients With Monofocal IOLs

B

Bucci Laser Vision Institute

Status

Completed

Conditions

Patient Satisfaction

Study type

Observational

Funder types

Other

Identifiers

NCT04134507
FAB-USA-001

Details and patient eligibility

About

Compare functional visual outcomes and patient satisfaction of post-LASIK patients having received presbyopia-correcting IOLs versus post-LASIK patients having received monofocal IOLs

Enrollment

44 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • 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

Trial design

44 participants in 2 patient groups

Extended Depth of Focus IOL
Description:
Post-LASIK patients with implantation of a presbyopia-correcting IOL
Monofocal IOL
Description:
Post-LASIK patients with implantation of a monofocal IOL

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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