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NCT02084212

Study of Retinal Sensitivity by Microperimetry During Epiretinal Membrane Surgery

Terminated NA Last updated 4 September 2019
What this trial tests

NA trial testing Microperimetry in Epiretinal Membrane Surgery in 6 participants. Terminated before completion.

Timeline
6 March 2013
Primary endpoint
24 April 2015
24 April 2015

Quick facts

Lead sponsorCentre Hospitalier Universitaire Dijon
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Enrollment6
Start date6 March 2013
Primary completion24 April 2015
Estimated completion24 April 2015
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Centre Hospitalier Universitaire Dijon

Who can join

18 and older, any sex, with Epiretinal Membrane Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Microperimetry

Trials testing the same drug.

Other recruiting trials for Epiretinal Membrane Surgery

Currently open trials in the same condition.

Other Centre Hospitalier Universitaire Dijon trials

Trials by the same sponsor.

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Data sources for this page

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