🏛️ Verified NIH Record • Updated 2024-09-25

Evaluation of Intraocular Pressure Following a Vitreoretinal Surgery Using Goldmann Applanation Tonometry, Icare and Accupen (NCT06522867)

Reliability Evaluation of Intraocular Pressure At Day 1 Following Vitreoretinal Surgery, Comparing Goldmann Applanation Tonometry (Gold Standard) to Icare and Accupen

🟢 Recruiting Observational / Diagnostic 📋 Clinical Research Protocol Sponsor: CHU de Quebec-Universite Laval

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Hôpital du Saint-Sacrement, CHU de Québec - Université Laval — Québec, Quebec

Age range: 18 Years

🧪 Interventions in This Study

  • Intraocular pressure measure (OTHER)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (1 Sites)

  • Hôpital du Saint-Sacrement, CHU de Québec - Université Laval — Québec, Quebec

📞 Contact the Study Coordinator

Phone: (418) 682-7511

Email: cuo.recherche@fmed.ulaval.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Intraocular Pressure

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗