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ENROLLING BY INVITATION
NCT07347379

Long-Term Clinical Outcomes Of Subjects Enrolled In The RxSight Light Adjustable Lens (LAL) And Light Delivery Device (LDD) New Enrollment Study

Sponsor: RxSight, Inc.

View on ClinicalTrials.gov

Summary

This is an observational, follow up study of subjects previously enrolled in the "RxSight Light Adjustable Lens (LAL) and Light Delivery Device (LDD) New Enrollment Study". The primary objective of this study is to collect long-term safety and effectiveness data on RxSight LAL and Control IOL in subjects previously implanted in the "RxSight Light Adjustable Lens (LAL) and Light Delivery Device (LDD) New Enrollment Study".

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

500

Start Date

2025-11-13

Completion Date

2026-09

Last Updated

2026-01-16

Healthy Volunteers

No

Interventions

DEVICE

Light Adjustable lens (LAL) and Light Delivery Device (LDD)

Experimental treatment group received Light adjustable lens with Light delivery Device treatments

DEVICE

Control IOL

Control treatment group received a Control IOL

Locations (1)

Focal Point Vision

San Antonio, Texas, United States