Actively Recruiting

Age: 18Years +
All Genders
NCT00532051

Intraocular Lens Power Calculation After Laser Refractive Surgery Based on Optical Coherence Tomography

Led by Oregon Health and Science University · Updated on 2024-02-12

690

Participants Needed

1

Research Sites

795 weeks

Total Duration

On this page

Sponsors

O

Oregon Health and Science University

Lead Sponsor

N

National Eye Institute (NEI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The long-term goal of this project is to utilize very high-speed optical coherence tomography (OCT) technology to guide surgical treatments of corneal diseases. OCT is well known for its exquisite resolution, but until recently it has not had sufficient speed to capture the shape of the cornea because of eye motion during OCT scanning. The development of Fourier-domain (FD) OCT technology has made the requisite speed possible. The objective of this project is to develop methods for imaging the cornea with an FD-OCT system that will precisely measure corneal shape and use this information to guide surgery. Cataract surgery in patients with previous laser vision correction often leads to significant near- or far-sightedness, a problem that could be resolved by using a more accurate intraocular lens power selection formula based on the measurement of corneal refractive power with OCT.

CONDITIONS

Official Title

Intraocular Lens Power Calculation After Laser Refractive Surgery Based on Optical Coherence Tomography

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients seeking cataract surgery with implantation of monofocal or toric intraocular lenses (not multifocal or accommodative IOLs)
  • Patients who have had previous laser vision correction procedures such as LASIK, PRK, LASEK, epi-LASIK, or radial keratectomy
  • Post-laser vision correction patients may be subdivided into those with previous hyperopic or myopic correction
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Unable to maintain stable fixation for OCT imaging
  • Unable to commit to all required study visits
  • Eyes with other eye diseases such as retinal disease, glaucoma, or other conditions that may limit visual outcome after surgery

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

Casey Eye Institute, Oregon Health & Science University

Portland, Oregon, United States, 97239

Actively Recruiting

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Research Team

H

Humberto Martinez, COT

CONTACT

D

Denny Romfh, OD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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