Navigated OCT Imaging With the P200TxE

Optos

Status: Completed

Conditions: Retinal Disease

Treatments: Device: Device: P200TxE

Study type: Interventional

Funder types: Industry

Identifiers

NCT04003831

OPT1033

Details and patient eligibility

About

The P200TxE will be used to obtain peripheral OCT (optical coherence tomography) images.

Enrollment: 26 patients

Sex: All

Ages: 22+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male or female subjects 22 years of age or older who have full legal capacity to volunteer on the date the informed consent is signed;
2. Subjects who can follow the instructions by the clinical staff at the clinical site,
3. Subjects who agree to participate in the study;
4. Subjects presenting with some form of peripheral retina pathology or retina pathology with peripheral manifestations.

Exclusion criteria

1. Subjects unable to tolerate ophthalmic imaging;
2. Subjects with ocular media not sufficiently clear to obtain acceptable OCT images;

Trial design

Primary purpose: Device Feasibility

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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26 participants in 1 patient group

Optical Coherence Tomographer

Other group

Treatment:

Device: Device: P200TxE