Epiretinal Membrane Clinical Trial
Official title:
Severe Foveal Epiretinal Membrane Contraction After Previous Fovea-sparing Internal Limiting Membrane Peeling Surgery
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 |
Verified date | June 2020 |
Source | Changhua Christian Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
To report cases who had received previous fovea-sparing internal limiting peeling membrane and developed secondary fovea epiretinal membrane contraction
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 |
Country | Name | City | State |
---|---|---|---|
Taiwan | Department of ophthalmology, Changhua Christian Hospital | Changhua City |
Lead Sponsor | Collaborator |
---|---|
Changhua Christian Hospital |
Taiwan,
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 |
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