Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

Visual and Patient Reported Outcomes With Clareon TruPlus

NCT: NCT07648355 · RECRUITING

NCT IDNCT07648355
StatusRECRUITING
Start Date2026-06-02
Completion2027-07-11
SponsorOVO LASIK + Lens (OTHER)
First posted
Last updated

Brief Summary

This is a prospective, single-site, two-surgeon, single-arm, observational study evaluating the Clareon TruPlus IOL. Subjects will be assessed up to 3 months post-operatively. Clinical evaluations will include refractive outcomes, visual acuity, and administration of the IOLSAT Questionnaire.

Frequently Asked Questions

What is Visual and Patient Reported Outcomes With Clareon TruPlus?

Visual and Patient Reported Outcomes With Clareon TruPlus is a clinical trial registered under NCT07648355. Current status: RECRUITING.

What is the status of NCT07648355?

The current status of NCT07648355 (Visual and Patient Reported Outcomes With Clareon TruPlus) is: RECRUITING.

When did Visual and Patient Reported Outcomes With Clareon TruPlus start?

Visual and Patient Reported Outcomes With Clareon TruPlus started on 2026-06-02.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

↑