Compare Visual Outcomes Using a New Diagnostic Device

Carl Zeiss Meditec

Status: Terminated

Conditions: Presbyopia

Treatments: Diagnostic Test: Diagnostic device

Study type: Observational

Funder types: Industry

Identifiers

NCT04037631

AT-LISA-tri 839MP BER-401-17

Details and patient eligibility

About

Evaluation of preoperative corrected distance visual acuity (CDVA) obtained with VirtIOL device compared to postoperative CDVA.

Enrollment: 24 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Patient informed of the consequences and constraints of the protocol and who has given his/her written informed consent

• Patients of any gender, aged 18 years to open age

• Assured follow-up examinations

• Healthy eyes without clinically significant age-related cataract

  -Exclusion Criteria:

• Patients unable to meet the limitations of the protocol or likely of non-cooperation during the trial

• Patients whose freedom is impaired by administrative or legal order

• Concurrent participation in another drug or device investigation

Trial design

24 participants in 1 patient group

Patients without clinically significant age-related cataract

Treatment:

Diagnostic Test: Diagnostic device