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Clinical Evaluation of Reproducibility of Keratometric Measurements and Influencing Factors in Cataract Patients — KerSty  

Cataract Clinical Trial

Official title:
Clinical Evaluation of Reproducibility of Keratometric Measurements and Influencing Factors in Cataract Patients

Clinical Trial Summary

The investigational device is an approved biometry device to perform biometric measurements preoperatively to calculate the needed IOL power.

First, two native measurements at the IOL Master will be performed. Thereafter randomly assigned artificial tears are instilled in the eye and biometry will be repeated within 30 seconds, as well as after 2 and 5 minutes.

At least 24hours after those measurements, two native measurements at the IOL Master will be performed. Thereafter, the not yet used artificial tears are instilled in the eye and biometry will be repeated within 30 seconds, as well as after 2 and 5 minutes.

Examinations will be implemented in accordance with the approved investigational plan on subjects and includes: repeated biometry without and with artificial tear drops.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04196621
Study type Interventional
Source Medical University of Vienna
Contact
Status Completed
Phase N/A
Start date January 1, 2019
Completion date February 15, 2020
View Details
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