Data Collection With the P200TE and P200TxE

Data Collection With the P200TE and P200TxE in Diseased Eyes for Clinical Developments

Status

Terminated

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05615896

Enrollment

Registered

2022-11-14

Start date

2021-04-22

Completion date

2022-06-17

Last updated

2024-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retinal Disease

Brief summary

The primary objective is to collect OCT scans on a modified P200TxE and P200TE.

Interventions

DEVICEImaging Session

Various scans will be captured on both devices

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

OTHER

Masking

NONE

Intervention model description

Eligibility

Sex/Gender

ALL

Age

22 Years to No maximum

Healthy volunteers

Inclusion criteria

: * Male or female volunteers 22 years of age or older who have full legal capacity to volunteer on the date the informed consent is signed; * Volunteers who can follow the instructions by the clinical staff at the clinical site; * Volunteers who agree to participate; * Volunteers who have been diagnosed with retina pathology with intra-retinal and/or subretinal fluid present in the posterior pole region.

Exclusion criteria

* Volunteers unable to tolerate ophthalmic imaging; * Volunteers with ocular media not sufficiently clear to obtain acceptable OCT images.

Design outcomes

Primary

Measure	Time frame	Description
Collection of images	1 year	The primary endpoint will be the collection of OCT scans on the P200TE and P200TxE devices. The scans will be used by R&D for development of a de-noising algorithm as well as other possible developments.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026