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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCHU de Quebec-Universite Laval

About this trial

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.

Eligibility criteria

Qualifiers

Age ≥ 18

Received a vitreoretinal surgery

Disqualifiers

Corneal dystrophy

Corneal surgery (penetrating keratoplasty, DSAEK/DMEK less than 6 months, radial keratotomy)

Irregular corneal surface

Active corneal ulcer

Trial design

Treatments tested in this trial

  • Intraocular pressure measure

Treatment groups

67 Participants
are divided into 1 treatment group

Sponsors and collaborators