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Study of Retinal Sensitivity by Microperimetry During Epiretinal Membrane Surgery

Study of Retinal Sensitivity by Microperimetry During Epiretinal Membrane Surgery

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02084212
Enrollment
6
Registered
2014-03-11
Start date
2013-03-06
Completion date
2015-04-24
Last updated
2019-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epiretinal Membrane Surgery

Brief summary

The aim of this research is to assess current care by studying macular function using microperimetry and by then comparing visual acuity results with OCT (Optical Coherence Tomography) data. The examinations performed are those usually done in the follow-up of epiretinal membrane surgery, apart from microperimetry which is an examination of the central visual field. Patients who undergo ERM surgery usually have a follow-up examination at 1 month, 3 months and 6 months after the surgery. The consultation includes an assessment of visual acuity, a fundus examination an SD-OCT of the retina. The present protocol will require no additional visits. The microperimetry will be done in addition to the usual follow-up examinations after ERM surgery.

Interventions

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Persons who have provided consent, * Patients about to undergo idiopathic epiretinal membrane surgery, * Patients undergoing first-line macular surgery

Exclusion criteria

* Persons not covered by national health insurance * Preexisting disease of macula/epiretinal membrane (ARMD, chorioretinal scarring) * Preoperative amblyopic eye * Insufficiently transparent media making it impossible to do the examinations

Design outcomes

Primary

MeasureTime frame
Change of visual acuity in ETDRS (Early Treatment Diabetic Retinopathy Study) scaleUp to 6 months after the operation.
Anomalies observed in the outer layers of retinaUp to 6 months after the operation
Evaluation of retinal sensitivity by microperimetryUp to 6 months after the operation

Secondary

MeasureTime frame
Abnormal surface autofluorescenceUp to 6 months after the operation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026