Zeiss® IOLMaster 700 Corneal Topography Module Comparison With Schwind's Sirius Corneal Topography®

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-01

Study Completion Date

2024-01-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

In order to determine the intraocular lens to be implanted during cataract surgery, keratometry and axial length must be measured in preoperative. The axial length is obtained by ocular ultrasound mode B. Keratometry is obtained by means of an automatic refractometer or corneal topography. Currently, ultrasound scanners are being developed with a topography module to combine axial length and keratometry measurement. The investigators want to evaluate the corneal topography module of the Zeiss® IOL Master 700 biometer.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

IOLMASTER 700 Central Topography Workflow Study.

NCT04875247

Cataract

COMPLETED

Comparability of Keratometry of VERION Image Guided System With Established Measuring Devices

NCT02377154

Healthy

COMPLETED NA

Repeatability, Reproducibility and Comparison of Cirrus OCT, RTVue OCT, MS-39 OCT, and Insight 100 VHFDU

NCT03473847

Corneal Thickness Measurement Epithelial Thickness Measurement LASIK Flap Thickness Measurement +1 more

SUSPENDED NA

Quality of Life Evaluation After Cataract Surgery Using 4 Types of Intraocular Lens Implant Combinations

NCT05376917

Cataract Intraocular Lens Implant

COMPLETED NA

Repeatability and Reproducibility of the IOLMaster 700 Vers 1.70 and Agreement With IOLMaster 700 Vers. 1.50 and Pentacam

NCT03518775

Cornea

COMPLETED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cataract

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Corneal Topography with IOLMaster and Sirius topography.

The experimental group will have the two exams: the topography with the IOLMAster and the topography with Sirius topography.

Group Type EXPERIMENTAL

measurement of axial length and keratometry by sonographers with a topographic module

Intervention Type OTHER

measurement of axial length and keratometry by sonographers with a topographic module

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

measurement of axial length and keratometry by sonographers with a topographic module

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Men and Women Requiring CHV Cataract Surgery
* Aged 18 or over
* Insured under a social security scheme
* Having been informed of the clinical study and having given oral express consent

Exclusion Criteria

* Person unable to express consent
* Patient with a history of corneal dystrophy, corneal refractive surgery or keratoconus.
* History of chronic corneal disease

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No