Axial Length Variability

Status Completed

Clinical Trial Summary

The accuracy of IOL calculation relies on the one hand on axial length measurements and on the other hand on corneal and lens thickness measurements.

AL difference in pre and postoperative measurements may be caused by changes of lens parameters.

Aim of this study is to evaluate the magnitude of changes in pre and postoperative measurements of AL.

Clinical Trial Description

This is a prospective observational, controlled and unmasked study that would include patients which undergo cataract presurgical examination, after patient signed written informed consent. For each patient only one eye will be included.

In total 50 eyes of 50 patients will be include. Due to missing previous data, the sample size is an approximation.

Prior to surgery, slit lamp examination and cataract grading (LOCS) is performed. Routine biometry is performed using the IOL Master 700 (Carl Zeiss Meditec AG, Jena, Germany) and Heidelberg Anterion (Heidelberg Engineering, Germany) for AL and lens measurement.

Additionally, evaluation of tilt and decentration will be performed using Purkinje meter device.

Follow-up examination will be performed three months after surgery and will contain: AL and lens measurement using the two ss-OCT biometery devices, lens evaluation (tilt and decentration of the IOL) using the Purkinje meter. Refractive outcome will be evaluated by determining best-corrected visual acuity and subjective refraction.

In women of childbearing age, a pregnancy test will be performed before inclusion into the study.

Main outcome variable:

• Extend of AL difference between pre- and postoperative measurements in both devices

Additional outcome variables:

- Agreement between the two ss-OCT devices in AL measurement

- Evaluation of lens parameter in AL differences between pre- and postoperative measurements

- Limit of agreement in lens tilt and decentration using two ss-OCT devices and Purkinje meter ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04580550
Study type	Interventional
Source	Vienna Institute for Research in Ocular Surgery
Contact
Status	Completed
Phase	N/A
Start date	November 1, 2019
Completion date	March 1, 2020

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