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NCT04445142 Clinical Trial

Fovea ERM After Fovea-sparing ILM Peeling

Epiretinal Membrane Clinical Trial

Official title:
Severe Foveal Epiretinal Membrane Contraction After Previous Fovea-sparing Internal Limiting Membrane Peeling Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04445142
Other study ID # 200402
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2019
Est. completion date April 30, 2020

Study information
Verified date June 2020
Source Changhua Christian Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Description:

Purpose: To report the rare complication of foveal epiretinal membrane (ERM) formation on residual internal limiting membrane (ILM) with severe contraction after previous fovea-sparing internal limiting membrane (ILM) peeling.

Study design: Retrospective case series Methods: We report patients who previously received fovea-sparing ILM peeling and complicated with foveal ERM formation and contraction.

Recruitment information / eligibility
Status Completed
Enrollment 3
Est. completion date April 30, 2020
Est. primary completion date April 30, 2020
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• fovea-sparing internal limiting membrane peeling
fovea-sparing internal limiting membrane peeling surgery

Locations
Country Name City State
Taiwan Department of ophthalmology, Changhua Christian Hospital Changhua City

Sponsors (1)
Lead Sponsor Collaborator
Changhua Christian Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual acuity Snellen visual acuity change 6 months
Primary Optical coherence tomography finding fovea change on optical coherence tomography 6 months
See also
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Terminated NCT04802265 - EpiRetinal Membrane Peeling and Internal Limiting Membrane