Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06522867

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

Led by CHU de Quebec-Universite Laval · Updated on 2024-09-26

67

Participants Needed

1

Research Sites

155 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Have received a vitreo-retinal surgery
Not Eligible

You will not qualify if you...

  • 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
  • History of scleral buckle

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hôpital du Saint-Sacrement, CHU de Québec - Université Laval

Québec, Quebec, Canada, G1S4L8

Actively Recruiting

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Research Team

J

Julie Mauger, BSc

CONTACT

S

Sébastien Méthot, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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