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Agreement of Two OCT Biometers: A Pilot Study
RecruitingObservational study
Who can join
Ages 21 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Have healthy, clear corneas for the normal cohort; * Have documented keratoconus for the keratoconus cohort; * Have reported use of daily contact lens use for the contact lens cohort; * Have documented dry eye, consisting of signs and symptoms for the dry eye cohort; * Has had previous keratorefractive surgery for the post-refractive surgery cohort; * Able to comprehend and sign the informed consent form. Exclusion Criteria: * Active ocular infection or inflammation; * Unable to fixate due to nystagmus or other eye movement abnormality (e.g., significant strabismus); * Any ocular disease and/or condition that, in the investigator's clinical judgment, may put the subject at significant risk, may compromise study result or may interfere significantly with the subject's participation in the study.
About the study
The purpose of this study is to compare the measurements obtained with two different biometers, UNITY Dx and Anterion. In eye care, a biometer is a device that uses laser technology to take highly precise measurements of the eye's internal structures. It is most frequently used to help determine the exact power of the intraocular lens (IOL) needed before cataract removal.
What is being tested
- UNITY DX (device)
- ANTERION (device)
Sponsor: Alcon Research · Participants: 50 · Started: Aug 17, 2026
Contact the study team
- Alcon Call Center · Phone: 1-888-451-3937
Official record on ClinicalTrials.gov — NCT07782619
Locations in the U.S.
| Utah | The Eye Institute of Utah, Salt Lake City |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.