Functional IOL Implantation in Patients With Epiretinal Membrane

Recruiting now · Not applicable

Conditions studied: Cataract, Intraocular Lens Complication, Epiretinal Membrane

In brief

We have designed this prospective study to evaluate macular involvement and epiretinal membrane (ERM) grading by OCT in eyes with ERM and to compare clinical outcomes after implantation of Enhance IOL with standard monofocal IOL in eyes with ERM grading preoperatively, aiming to find out whether functional IOL is benefit for patients with ERM.

Key facts

Study ID

NCT06719739

Run by

Eye & ENT Hospital of Fudan University

People needed

90

Starts

2024-09-21

Expected to finish

2026-09-21

Last updated by the study team

2026-04-08

Who can join

Age: 20 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Requirement for cataract extraction
• Age > 40 years
• Axial length in 21mm to 25mm
• ERM

You may not qualify if…

• Residual corneal astigmatism > 1.0 D
• Amblyopia
• Previous ocular surgery
• Other ocular pathologies apart from mERM, such as diabetic retinopathy, macular degeneration, glaucoma with field defects
• Requirements for further ocular surgery (other than Nd:YAG capsulotomy) or retinal laser treatments during the study

Where it is running

• Eye and Ear, Nose, and Throat Hospital of Fudan University — Shanghai, Shanghai Municipality, China (enrolling)
• Shanghai Heping Eye Hospital — Shanghai, Shanghai Municipality, China (enrolling)

Full record on ClinicalTrials.gov

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