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Change of aniseikonia and retinal displacement after vitrectomy according to symptom duration in epiretinal membrane

Change of aniseikonia and retinal displacement after vitrectomy according to symptom duration in epiretinal membrane

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008079
Enrollment
75
Registered
2023-01-04
Start date
2021-02-14
Completion date
Unknown
Last updated
2023-02-08

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

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Epiretinal membrane patients over 20-year-old who are planned to undertake pars plana vitrectomy Patients who have over 2' of aniseikonia either horizontal or vertical plane in the preoperative aniseikonia test. Patients who have signed and agreed to the informed consent/

Exclusion criteria

Exclusion criteria: Patients who have epiretinal membrane in the fellow eye. Patients who have any macular disorder in the fellow eye. Patients who underwent intraocular surgery in any eye (except surgery for cataract). Patients who have high myopia or history of refractive surgery in any eye.

Design outcomes

Primary

MeasureTime frame
The postoperative change of aniseikonia according to symptom duration;The postoperative tangential displacement of retina according to symptom duration—

Secondary

MeasureTime frame
The association between postoperative change of aniseikonia and tangential displacement of retina—

Countries

Korea, Republic of

Contacts

Public ContactJaehwan Choi

Samsung Medical Center

jae8903@gmail.com+82-2-3410-6776

Outcome results

None listed

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