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Visual Outcomes after implanting the bilateral PureSee emmetropia and -0.5D mini-monovision mix-match

Visual Outcomes after implanting the bilateral PureSee emmetropia and -0.5D mini-monovision mix-match

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011059
Enrollment
30
Registered
2025-09-23
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-11-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : 1. Study Design Previous studies have reported that implantation of extended depth of focus (EDOF) intraocular lenses (IOLs) similar to the PureSee IOL with a mini-monovision strategy

Sponsors

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Adults (male or female) aged =45 years scheduled to undergo cataract surgery - Overall healthy condition - Eyes without any ocular disease other than cataract - Pupil dilation =6 mm - Ability to read and fully understand the provided informed consent document in Korean, in compliance with HIPAA regulations

Exclusion criteria

Exclusion criteria: - Age =75 years - Pregnant or breastfeeding women - History of prior ocular surgery (including intraocular, refractive, or ocular surface surgery) or ocular trauma - Evidence of keratoconus or characteristic irregular astigmatism on preoperative corneal topography - Contact lens wear within the specified washout period: PMMA lenses within 6 months, RGP lenses within 1 month, or disposable soft lenses within 1 week prior to surgery - Presence of ocular conditions that may affect the anterior chamber or lens stability (e.g., pseudoexfoliation syndrome, traumatic cataract, Marfan syndrome) - Visual field test showing generalized visual field loss, absence of preserved central vision, or evidence of progressive visual field defects - Inability to read or understand the informed consent document in Korean (e.g., illiteracy or non-Korean speaking individuals)

Design outcomes

Primary

MeasureTime frame
Uncorrected visual acuity (UCVA) at near, intermediate, and distance;best-corrected visual acuity (BCVA) at near, intermediate, and distance;patient satisfaction will be assessed using the questionnaire provided by the Korean Society of Cataract and Refractive Surgery (KSCRS)

Secondary

MeasureTime frame
binocular defocus curves and contrast sensitivity

Countries

Korea, Republic of

Contacts

Public ContactSo-Hyang Chung

The Catholic University of Korea, Seoul St. Mary's Hospital

chungsh@catholic.ac.kr+82-2-2258-6203

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026