Evaluating the Safety of the SPECTRALIS CENTAURUS Device

Retinal Diseases Clinical Trial

— CENTAURUS  

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 Details — Status: Recruiting

Administrative data

• NCT number: NCT04968756
• Other study ID #: CENTAURUS
• Status: Recruiting
• Phase: N/A
• Start date: September 9, 2021
• Est. completion date: December 2025

Study information

• Verified date: January 2024
• Source: Insel Gruppe AG, University Hospital Bern
• Contact: Martin Zinkernagel, MD PhD
• Phone: +41 (0)31 632 85 03
• Email: martin.zinkernagel[@]insel.ch
• Is FDA regulated: No
• Study type: Interventional

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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: December 2025
• Est. primary completion date: December 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 95 Years

Eligibility

Inclusion Criteria:

• Written Informed Consent
• For Stage 1, any patient aged >18 years with the need for conventional laser retina ablation
• For Stage 2, will be restricted to people aged 50 to <95 years with lesion characteristics that meet the criteria for intermediate AMD

Exclusion Criteria:

• Presence of reticular pseudodrusen
• Any manifestation of late-stage AMD
• Known hypersensitivity or allergy to fluorescein or uncontrolled hypertension
• Concomitant systemic corticosteroid treatment for continuous period longer than 2 weeks
• History of any vitreous haemorrhage within 4 weeks prior to screening or current haemorrhage in the study eye
• Inability to obtain fundus photographs or fluorescein angiogram of sufficient quality
• Photosensitive epilepsy
• Insufficient retinal pigmentation (albinism)
• Corneal opacity / lens opacity
• Women of child-bearing potential
• Contralateral eye is at an advanced stage of disease and has poor visual acuity
• Inability to follow the procedures of the study
• Participation in another study with investigational drug within the 30 days preceding and during the present study - Inability or lack of willingness to commit to return for all clinical visits and complete all study-related procedures

Related Conditions & MeSH terms

• Retinal Diseases

Intervention

Device:
• Selective retina therapy SPECTRALIS CENTAURUS device
Microsecond laser microsurgery by using the SPECTRALIS CENTAURUS device

Locations

Country	Name	City	State
Switzerland	University Hospital Inselspital	Bern

Sponsors (2)

Lead Sponsor	Collaborator
Insel Gruppe AG, University Hospital Bern	Bern University of Applied Sciences

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety SPECTRALIS CENTAURUS - AEs	The primary objective of this study is to assess the safety of the SPECTRALIS CENTAURUS device in clinical use by the evaluation of any adverse events (AEs) that may be related to the study device or the study intervention, including device deficiencies (DDs); The following potential AEs are evaluated throughout the study regarding the laser treatment: Decrease in visual acuity; Choroidal neovascularization at treatment location (laser lesion); Transient increased edema / decreased vision; Development or worsening of macular edema; Bruch's membrane rupture; Retinal and choroidal haemorrhage; Inadvertent foveal burns	26 weeks
Primary	Safety SPECTRALIS CENTAURUS - DDs	In addition to the AEs, the following potential device deficiencies (DDs) can be listed in relation to the treatment and the SPECTRALIS CENTAURUS device: Unintentional laser delivery; Unintentional OCT (M-scan) failure during the treatment; Unintentional scanning laser ophthalmoscope (SLO) failure during the treatment; Unintentional treatment software failure during the treatment; Unintentional treatment laser failure during the treatment; Basic system failure during the treatment; Beside the DDs mentioned above, additional sub-criteria are assessed by default in advance to the treatment visit according to an acceptance test protocol (ATP). The ATP establishes the acceptance test framework for the SPECTRALIS CENTAURUS and describes the scope of the work performed and the approach taken to validate that the system performs as required. An acceptance test is carried out on each day on which a patient is to be treated.	At treatment (baseline)
Secondary	Evaluation of OCT for SRT dosimetry	During treatment, OCT M-scans are recorded collinear to the treatment laser application. Post-treatment, all lesions are examined by fluorescein angiography (FA) for RPE cell damage. In addition, the OCT-M scan data is examined for fringe washouts (signal washouts) that occur with RPE cell damage. An analysis of these data (RPE cell damage vs. OCT fringe washouts) will reveal whether OCT is suitable for real-time dosimetry of SRT.	At treatment (baseline)
Secondary	Progression of AMD after laser treatment according to best-corrected visual acuity (BCVA)	Course of disease monitoring on AMD and confluent soft drusen with BCVA: Visual acuity is assessed using the Early Treatment Diabetic Retinopathy Study (ETDRS) chart (consisting of rows of letters) / LogMAR chart (Logarithm of the Minimum Angle of Resolution), after appropriate refraction. Visual acuity represents the basic and most clinically relevant functional test to evaluate of central visual acuity.	At treatment (baseline) and after 1, 4, 12 and 26 weeks
Secondary	Progression of AMD after laser treatment according to OCT imaging	Course of disease monitoring on intermediary AMD and confluent soft drusen with OCT: OCT provides non-invasive morphological assessment of the retinal layers including the RPE and the choroid. It is a commonly used objective method during clinical assessment. OCT allows to identify structural changes such as Bruch's membrane ruptures, choroidal neovascularizations (CNV) with exudative macular edema, photoreceptor damage and drusen evolution. A macular volume OCT scan centered at the fovea will be acquired routinely. Additionally, volume OCT scans across the laser area will be acquired. This allows, for example, that a change in retinal thickness (µm) can be observed in the short term as well as in the long term. No single endpoint is given for this examination. However, experience shows that CNV would be the most likely case which can be expected with this laser treatment.	At treatment (baseline) and after 1, 4, 12 and 26 weeks
Secondary	Progression of AMD after laser treatment according to FA imaging	Course of disease monitoring on intermediary AMD and confluent soft drusen with FA: Fluorescein is injected intravenously before serial fundus image are taken after excitation of the fluorescein dye. No single endpoint is given for this examination. However, experience shows that CNV and subtle laser scars would be the most likely cases which can be expected with this laser treatment.	At treatment (baseline) and after 12 weeks
Secondary	Progression of AMD after laser treatment according to color fundus photography (CFP)	Course of disease monitoring on intermediary AMD and confluent soft drusen with CFP: CFP will be used to document and monitor pigmentary changes of the fundus and potential formation of scars after laser application. Since it is difficult to quantify fundus image changes, the principal investigator as well as a safety committee will evaluate fundus changes on an individual basis, taking into account the location and laser parameters used in the participant.	At treatment (baseline) and after 1, 4, 12 and 26 weeks