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Evaluation of Intraocular Pressure Following a Vitreoretinal Surgery Using Goldmann Applanation Tonometry, Icare and Accupen

RecruitingNAAges 18 Years - anyAllCHU de Quebec-Universite Laval
NCT06522867 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of this prospective controlled study is to measure the reliability of two intraocular pressure (IOP)-measuring instruments in comparison to the gold standard, Goldmann applanation tonometry (GAT) following vitreo-retinal surgery. The main question the current study aims to answer is: are Icare and Accupen as accurate as GAT in measuring IOP one day post eye surgery? Participants in this study will have their IOP measured by the three different instruments one day post-surgery.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Age ≥ 18 * Received a vitreoretinal surgery Exclusion Criteria: * Corneal dystrophy * Corneal surgery (penetrating keratoplasty, DSAEK/DMEK less than 6 months, radial keratotomy) * Irregular corneal surface * Active corneal ulcer * Active epithelial deficit * Central corneal scarring * A history of scleral buckle
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What it tests

  • Intraocular pressure measure
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Where

1 site
Hôpital du Saint-Sacrement, CHU de Québec - Université Laval
Québec, Canada
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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