MedTrace Logo

IOLMASTER 700 Central Topography Workflow Study.

NCT04875247 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2023-02-17

No results posted yet for this study

Summary

The use of ocular biometers like IOLMaster 700, is a common practice to identify several ocular parameters such as the keratometry of the cornea and the axial length of the eye, which are necessary for calculating the power of the intraocular lens in cataract surgery. However, the additional use of other devices, such as Cassini and Pentacam is used to obtain more information of the central topography of the eye. Recently, a new version of the IOLMaster 700 equipment that provides much more detailed information than in its previous version has been presented. The objective of this study is to measure the time that the new IOLMaster 700 takes to perform these measurements of the central topography and compare it with the time it takes using the central topography using the standard IOLMaster 700 version with Cassini on one hand and Pentacam on the other.

It is hypothesized that the use of the new version of the IOLMaster 700 equipment alone can reduce the time of measurements and improve the clinic workflow.

Conditions

  • Cataract

Interventions

DEVICE

IOLMaster 700 with central topography

The time needed to perform the measurement using the IOLMaster700 equipment with central topography will be recorded.

DEVICE

IOLMaster 700 without central topography plus Cassini

The time needed to perform the measurement using the IOLMaster700 equipment without central topography plus the Cassini equipment will be recorded.

DEVICE

IOLMaster 700 without central topography plus Pentacam

The time needed to perform the measurement using the IOLMaster700 equipment without central topography plus the Pentacam equipment will be recorded.

Sponsors & Collaborators

  • OFTALVIST (Oftalmología Vistahermosa S.L)

    lead INDUSTRY

Principal Investigators

  • Ramón Ruiz Mesa., Doctor · OFTALVIST (Oftalmología Vistahermosa S.L)

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-12
Primary Completion
2021-09-09
Completion
2021-09-09

Countries

  • Spain

More Related Trials

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 NCT04875247 on ClinicalTrials.gov