CompletedNot Applicable

Fovea ERM After Fovea-sparing ILM Peeling

Taiwan3 participantsStarted 2019-09-01

Plain-language summary

To report cases who had received previous fovea-sparing internal limiting peeling membrane and developed secondary fovea epiretinal membrane contraction

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * patients who developed secondary fovea epiretinal membrane after previous fovea-sparing internal limiting membrane surgery Exclusion Criteria: * patients who did not receive previous fovea-sparing internal limiting membrane surgery

What they're measuring

Visual acuity

Timeframe: 6 months

Optical coherence tomography finding

Timeframe: 6 months

Trial details

NCT IDNCT04445142

SponsorChanghua Christian Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-04-30

View on ClinicalTrials.gov More Epiretinal Membrane trials