IOLMASTER 700 Central Topography Workflow Study.

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-05-12

Study Completion Date

2021-09-09

Brief Summary

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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.

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Detailed Description

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Conditions

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Cataract

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Single arm

All patients will be assigned to this cohort.

IOLMaster 700 with central topography

Intervention Type DEVICE

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

IOLMaster 700 without central topography plus Cassini

Intervention Type DEVICE

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

IOLMaster 700 without central topography plus Pentacam

Intervention Type DEVICE

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

Interventions

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IOLMaster 700 with central topography

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

Intervention Type 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.

Intervention Type 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.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients that have to undergo a cataract surgery
* Patients older than 50 years.

Exclusion Criteria

* Patients that have already undergone a previous corneal surgery.
* Patients suffering from keratoconus.
* Patients exhibiting corneal scars
* Patients exhibiting pterygium

Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No