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Assessing Agreement Between Acuvera Capture and Paper-Based Methods for BCVA Data Recording in Ophthalmic Trials

NCT07613580 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 90

Last updated 2026-05-29

No results posted yet for this study

Summary

Study Purpose: To evaluate the level of agreement between the Acuvera Capture application and traditional paper-based methods for recording Best Corrected Visual Acuity (BCVA) in ophthalmic clinical trials. The study aims to determine whether the electronic capture system provides equivalent or improved accuracy, consistency, and error reduction compared with paper-based recording, thereby supporting its potential adoption as a reliable method for BCVA data collection in clinical research.

Conditions

  • Ophthalmopathy

Sponsors & Collaborators

  • OptymEdge, LLC

    lead INDUSTRY

Principal Investigators

  • Ana Rita Santos, PhD · OptymEdge, LLC

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-01-12
Primary Completion
2026-06-30
Completion
2026-06-30

Countries

  • Portugal

Study Locations

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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 NCT07613580 on ClinicalTrials.gov