Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL)

Completed

Conditions studied: Cataract, Pseudophakia

In brief

The objective of this investigator initiated study (IIT-001) is to obtain data on clinical methods which can be used during the examination of patients desiring binocular custom vision with the Light Adjustable Lens (LAL). An analysis of the collected data will be performed to determine whether these clinical assessments can be used by doctors to enhance their patient's clinical outcome.

Key facts

Study ID

NCT04533191

Run by

Vance Thompson Vision

People needed

25

Starts

2020-09-01

Expected to finish

2021-02-01

Last updated by the study team

2024-05-20

Who can join

Age: 18 and older, up to 110. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients able to sign informed consent
• Patients who plan to undergo bilateral implantation with the commercial LAL and receive binocular custom vision are eligible for study participation.

You may not qualify if…

• Inability to sign informed consent
• Any pathology for which, in the investigator's judgement, could reduce the subjects BCVA
• Unable to return for light treatments

Where it is running

• Vance Thompson Vision — Sioux Falls, South Dakota, United States

Full record on ClinicalTrials.gov

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