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UNITY DX Cornea Study

Alcon Research · NCT07768735

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 22+ · All sexes
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
110
US sites recruiting
1
Study start
September 24, 2026
Record last updated
October 1, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: UNITY DX; ANTERION

Conditions: Tomography

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full 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.

Recruiting US locations

Study contacts (from the official record)

  • Alcon Call Center · 1-888-451-3937 · alcon.medinfo@alcon.com
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UNITY DX Cornea Study (NCT07768735) | Bored Studies