Compare Visual Outcomes Using a New Diagnostic Device

NCT04037631 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2021-01-28

No results posted yet for this study

Summary

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

Conditions

Interventions

DIAGNOSTIC_TEST

Diagnostic device

Diagnostic test

Sponsors & Collaborators

  • Carl Zeiss Meditec AG

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-20
Primary Completion
2020-05-01
Completion
2020-05-01

Countries

  • Germany

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04037631 on ClinicalTrials.gov