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Evaluating the Safety of the SPECTRALIS CENTAURUS Device — CENTAURUS  

Retinal Diseases Clinical Trial

Official title:
Open Label Early Feasibility Study Evaluating the Safety of the SPECTRALIS CENTAURUS Device for Dosimetry of Selective Retina Therapy With Optical Coherence Tomography

Clinical Trial Summary

The objective of this clinical trial is to evaluate the safety of the SPECTRALIS CENTAURUS device (HuCE-optoLab, BFH TI, Biel, CH) in a clinical setting on patients with retinal diseases.

Clinical Trial Description

Optical microsurgery of the retinal pigment epithelium (RPE) requires reliable real-time dosimetry to prevent unwanted overexposure of the neuroretina. The SPECTRALIS CENTAURUS device implements optical coherence tomography (OCT) to detect intentional elimination of RPE cells caused by a prototype laser for selective retina therapy (SRT). Within this clinical trial the safety of the SPECTRALIS CENTAURUS device and its ability to detect RPE cell damage towards selective real-time laser microsurgery will be evaluated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04968756
Study type Interventional
Source Insel Gruppe AG, University Hospital Bern
Contact Martin Zinkernagel, MD PhD
Phone +41 (0)31 632 85 03
Email martin.zinkernagel@insel.ch
Status Recruiting
Phase N/A
Start date September 9, 2021
Completion date December 2025
View Details
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