Intraindividual Comparison of Two Non- Diffractive Extended Depth of Focus Intraocular Lenses Set for Emmetropia

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Intra-individual comparison of the PureSee EDOF IOL with the Acunex Vario EDOF IOL set for emmetropia.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Maximum Age: 105
Healthy Volunteers: f
View:

• Age-related bilateral cataract

• Age 21 or older

• Visual acuity \> 0.05

• For patients with regular corneal astigmatism greater than or equal to 1.00 dpt toric IOLs will be implanted

• Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically relevant

• Written informed consent prior to surgery

Locations
Other Locations
Austria
Vienna Institute for Research in Ocular Surgery (VIROS), Hanusch Hospital Vienna
RECRUITING
Vienna
Contact Information
Primary
Johannes Zeilinger, MD
office@viros.at
01 91021 57564
Backup
Manuel Ruiss, MSc
office@viros.at
01 91021 57564
Time Frame
Start Date: 2024-07-29
Estimated Completion Date: 2026-07-01
Participants
Target number of participants: 40
Treatments
Experimental: Acunex Vario AN6V
Patients will receive the Acunex IOL during cataract surgery
Experimental: PureSee
Patients will receive the PureSee IOL during cataract surgery
Related Therapeutic Areas
Sponsors
Leads: Vienna Institute for Research in Ocular Surgery

This content was sourced from clinicaltrials.gov