πŸ›οΈ Verified NIH Record β€’ Updated 2025-01-29

Refractive Outcomes Utilizing Two SS-OCT Biometers for IOL Power Calculations (NCT06801678)

🟒 Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: The Eye institute of Utah

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

The purpose of this study is to evaluate and compare the potential refractive outcomes using the Argos 1.5 biometer in the surgical planning for cataract extraction to that obtained from IOLMaster 700. Both devices are used as standard of care in surgical planning optimization for patients undergoing cataract surgery.

Who can join: Review the eligibility criteria below.

Location: The Eye Institute of Utah β€” Salt Lake City, Utah

Age range: 21 Years

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (1 Sites)

  • The Eye Institute of Utah β€” Salt Lake City, Utah

πŸ“ž Contact the Study Coordinator

Phone: (801) 263-5705

Email: lguild@theeyeinstitute.com

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

πŸ’° 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 Β§ 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.

Explore by condition: All Cataract clinical trials

πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—