Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06522867

Reliability Evaluation of Intraocular Pressure One Day After Vitreoretinal Surgery Comparing Goldmann Applanation Tonometry to Icare and Accupen

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

67

Participants Needed

1

Research Sites

134 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the accuracy of two portable instruments, Icare and Accupen, for measuring intraocular pressure (IOP) compared to the gold standard, Goldmann applanation tonometry (GAT), one day after vitreoretinal surgery. The study aims to determine if these simpler, easier-to-use methods provide reliable IOP measurements in post-operative patients, helping to potentially replace the more cumbersome GAT method. This prospective controlled study enrolls 67 patients who have undergone vitreoretinal surgery. Participants will have their IOP measured using three devices: GAT, Icare, and Accupen, in a randomized order during their one-day post-operative visit. A resident ophthalmologist will perform two pressure measurements with each device and calculate the average for comparison. The study focuses on verifying if the portable methods match the accuracy of GAT in this surgical context. During the single post-operative visit, medical history related to the eye surgery and diagnosis will be recorded. The main outcome is to assess the agreement of IOP measurements among the three devices one day after surgery. The study will also evaluate the reliability and validity of the portable devices across different pressure levels. Participation involves this one-time measurement and medical review, with no long-term follow-up required.

CONDITIONS

Brief 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 vitreoretinal surgery
Not Eligible

You will not qualify if you...

  • Corneal dystrophy
  • Corneal surgery such as penetrating keratoplasty or DSAEK/DMEK within the last 6 months
  • Irregular corneal surface
  • Active corneal ulcer
  • Active epithelial deficit
  • Central corneal scarring
  • History of scleral buckle surgery on the eye involved

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - 1 day

Participants undergo vitreoretinal surgery followed by immediate post-operative care.

1 post-operative visit (in-person)

Trial Site Locations

Total: 1 location

1

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

Québec, Quebec, Canada, G1S4L8

Actively Recruiting

Loading map...

Research Team

J

Julie Mauger, BSc

S

Sébastien Méthot, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

Similar Trials

Effect of Position and Anesthetic Choice on Intraocular Pres...

Intraocular Pressure

Actively Recruiting

1 location

Effect of Raised End-Tidal pCO2 on Choroidal Volume in Child...

Intraocular Pressure

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here