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IOLMASTER 700 Central Topography Workflow Study.

IOLMASTER 700 Central Topography Workflow Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04875247
Enrollment
100
Registered
2021-05-06
Start date
2021-05-12
Completion date
2021-09-09
Last updated
2023-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract

Brief 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.

Interventions

DEVICEIOLMaster 700 with central topography

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

DEVICEIOLMaster 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.

DEVICEIOLMaster 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

OFTALVIST (Oftalmología Vistahermosa S.L)
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Time needed to do the measurements with each equipment1 day (Cataract pre-surgery visit)Time needed to do the measurements with each equipment

Secondary

MeasureTime frameDescription
Central topography1 day (Cataract pre-surgery visit)Measurement of keratometry (K): Flat Keratometry (K1) and Steep Keratometry (K2)

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026