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

This trial does not accept healthy volunteers

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

Design model

Single group

Treatments tested in this trial

  • Intraocular pressure measure

    Other intervention

    The intraocular pressure of the subjects using either the Goldmann applanation tonometer, Icare or Accupen. The order of the measure is randomized.

Treatment groups

67 Participants
are divided into 1 treatment group
Group A: Intraocular pressure measureExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Absence of difference between intracular pressure measured by devices

No difference in the intraocular pressure measured by Accupen or Icare compared to Goldmann tonometer.

Time frame
at the post-operative visit (1 day after surgery)

Secondary outcomes

1

Reliability and validity of devices at all intracular pressure level

The devices have the same intraocular pressure measured by Goldmann tonometer at High level of pressure (\>24mmHg), moderate level (10-24mmHg) and low level (\<10mmHg).

Time frame
at the post-operative visit (1 day after surgery)

Other outcomes

Sponsors and contacts

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