Home › Keratoconus › NCT07768735
UNITY DX Cornea Study
RecruitingObservational studyHealthy volunteers welcome
UNITY DX Cornea Precision and Agreement Study
Who can join
Ages 22 and older · All sexes · Healthy volunteers welcome
Full eligibility criteria
Key Inclusion Criteria: * Able to understand and sign an Institutional Review Board approved informed consent form. * Willing and able to attend all scheduled study visits as required per protocol. * Identified by the investigator as having normal corneas or abnormal corneas per protocol-specified criteria. * Other protocol-specified inclusion criteria may apply. Key Exclusion Criteria: * Unable to fixate due to nystagmus or other eye movement abnormality, such as significant strabismus. * Any ocular disease and/or condition that, in the investigator's clinical judgement, may put the subject at significant risk, may compromise study results, or may interfere significantly with the subject's participation in the study. * Active ocular infection or inflammation. * Other protocol-specified exclusion criteria may apply.
About the study
The purpose of this study is to validate the clinical measurement performance of an investigational biometer. Subjects will undergo multiple measurements of the eye, and the agreement, repeatability, and reproducibility of corneal and epithelial thickness maps will be evaluated.
What is being tested
- UNITY DX (device)
- ANTERION (device)
Sponsor: Alcon Research · Participants: 110 · Started: Sep 24, 2026
Contact the study team
- Alcon Call Center · Phone: 1-888-451-3937
Official record on ClinicalTrials.gov — NCT07768735
Locations in the U.S.
| Utah | The Eye Institute of Utah, Salt Lake City |
Conditions
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.