Fovea ERM After Fovea-sparing ILM Peeling
Sponsor
Changhua Christian Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04445142
Collaborator
(none)
3
1
8
0.4
Study Details
Study Description
Brief Summary
To report cases who had received previous fovea-sparing internal limiting peeling membrane and developed secondary fovea epiretinal membrane contraction
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed 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.
Study Design
Study Type:
Observational
Actual Enrollment
:
3 participants
Observational Model:
Case-Only
Time Perspective:
Retrospective
Official Title:
Severe Foveal Epiretinal Membrane Contraction After Previous Fovea-sparing Internal Limiting Membrane Peeling Surgery
Actual Study Start Date
:
Sep 1, 2019
Actual Primary Completion Date
:
Apr 30, 2020
Actual Study Completion Date
:
Apr 30, 2020
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| epiretinal membrane group Patients developed secondary fovea epiretinal membrane |
Procedure: fovea-sparing internal limiting membrane peeling
fovea-sparing internal limiting membrane peeling surgery
|
Outcome Measures
Primary Outcome Measures
- Visual acuity [6 months]
Snellen visual acuity change
- Optical coherence tomography finding [6 months]
fovea change on optical coherence tomography
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
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
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Department of ophthalmology, Changhua Christian Hospital | Changhua City | Taiwan | 500 |
Sponsors and Collaborators
- Changhua Christian Hospital
Investigators
- Study Chair: San-Ni Chen, MD, Changhua Christian Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
San Ni Chen,
Head of department of ophthalmology,
Changhua Christian Hospital
ClinicalTrials.gov Identifier:
NCT04445142
Other Study ID Numbers:
- 200402
First Posted:
Jun 24, 2020
Last Update Posted:
Jun 24, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by San Ni Chen,
Head of department of ophthalmology,
Changhua Christian Hospital
Additional relevant MeSH terms: