Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07142785

Clinical Evaluation of With or Without Internal Limiting Membrane Peeling for Idiopathic Epiretinal Membrane Surgery: A Randomized Controlled Trial

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2025-08-27

96

Participants Needed

1

Research Sites

147 weeks

Total Duration

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AI-Summary

What this Trial Is About

Idiopathic epiretinal membrane (ERM) is an age-related degenerative retinal condition. One of the primary treatment approaches is vitrectomy combined with epiretinal membrane peeling. However, whether to concurrently perform internal limiting membrane (ILM) peeling remains clinically controversial. Therefore, this study aims to compare the efficacy and safety of performing versus omitting ILM peeling during idiopathic ERM surgery.

CONDITIONS

Official Title

Clinical Evaluation of With or Without Internal Limiting Membrane Peeling for Idiopathic Epiretinal Membrane Surgery: A Randomized Controlled Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged >18 years presenting to our hospital within the study period.
  • Patients diagnosed with idiopathic epiretinal membrane (ERM) based on examination.
  • Patients with best-corrected visual acuity (BCVA) �3C= 0.6 or the presence of metamorphopsia.
Not Eligible

You will not qualify if you...

  • Patients with secondary ERM identified during preoperative evaluation (e.g., secondary to retinal vein occlusion).
  • Patients with concomitant ocular diseases affecting the macula, such as macular degeneration, macular schisis, or macular atrophy.
  • Patients with a history of ocular trauma or previous ocular surgery (except for cataract surgery).
  • Patients with severe systemic diseases contraindicated for surgery.
  • Patients with poor compliance or concomitant psychiatric disorders.
  • Patients who participated in other clinical trials during the follow-up period or who were lost to follow-up.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Eye Center of the Second Affiliated Hospital of Zhejiang University

Hangzhou, Zhejiang, China, 310058

Actively Recruiting

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Research Team

Y

Yueyang Zhong, MD.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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