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Agreement of Ocular Biometry and Intraocular Lens Power Between OA-2000 and Pentacam AXL in Cataract Patients

NCT07500272 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 94

Last updated 2026-03-30

No results posted yet for this study

Summary

This study aim to evaluate the agreement of ocular biometric parameters and intraocular lens between two devices (OA-2000 and Pentacam AXL) in patients with cataract.

Participants will be measured ocular biometric parameters once with each device in a random order by the same experienced operator.

Conditions

  • Cataract
  • Intraocular Lens

Interventions

DEVICE

Swept-source optical coherence tomography with Placido-disc topography

Measurement technology using swept-source optical coherence tomography with Placido-disc topography

DEVICE

Scheimpflug tomography with partial coherence interferometry

Measurement technology using Scheimpflug tomography with partial coherence interferometry

Sponsors & Collaborators

  • Burapha University

    lead OTHER

Principal Investigators

  • Rosepon Asawaworarit, M.D., M.Sc. · Burapha University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-02
Primary Completion
2024-11-29
Completion
2024-11-29

Countries

  • Thailand

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 NCT07500272 on ClinicalTrials.gov