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Clinical outcomes of implantable collamer lens implantation without use of an ophthalmic viscoelastic device

Clinical outcomes of implantable collamer lens implantation without use of an ophthalmic viscoelastic device

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0004929
Enrollment
50
Registered
2020-04-16
Start date
2020-04-15
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

None listed

Interventions

None listed

Sponsors

Onnuri Smile Ophthalmic Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: a corrected distance visual acuity of 20/40 or better, stable bilateral myopia for at least 2 years, refractive error in the correctable range [from -0.50 to -18.00 diopters (D)], and a clear cornea

Exclusion criteria

Exclusion criteria: anterior chamber depth = 2.8 mm, endothelial cell density = 2,000 cells/mm2, mesopic pupil > 7.0 mm, cataract, and a history of any ophthalmic surgery or disease

Design outcomes

Primary

MeasureTime frame
Intraocular pressure;endothelial cell density—

Secondary

MeasureTime frame
uncorrected visual acuity;manifest refraction—

Countries

Korea, Republic of

Contacts

Public ContactBu Ki Kim

Onnuri Smile Ophthalmic Clinic

Outcome results

None listed

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