Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL)

Vance Thompson Vision

Status: Completed

Conditions: Pseudophakia; Cataract

Treatments: Procedure: LAL IOL lens

Study type: Observational

Funder types: Other

Identifiers

NCT04533191

IIT-001

Details and patient eligibility

About

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.

Enrollment: 25 patients

Sex: All

Ages: 18 to 110 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• 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

Trial design

25 participants in 1 patient group

Subjects treated with LAL lens

Description:

Subjects that underwent standard of care cataract surgery and LAL IOL placement.

Treatment:

Procedure: LAL IOL lens