Data Collection With the P200TE and P200TxE

Not Applicable

Terminated

• Conditions: Retinal Disease
• Interventions: Device: Imaging Session

• Registration Number: NCT05615896
• Lead Sponsor: Optos, PLC

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2021-04-22
• Primary Completion: 2021-04-28
• Study First Submitted: 2021-06-21
• Study Completion: 2022-06-17
• Study First Submitted QC: 2022-11-08
• Study First Posted: 2022-11-14
• Status Verified: 2024-03
• Last Update Submitted: 2024-03-08
• Last Update Posted: 2024-03-12

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 5

Inclusion Criteria

Not provided

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
P200TxE Device First	Imaging Session	-
P200TE Device First	Imaging Session	-

Primary Outcome Measures

Name	Time	Method
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.

Trial Locations

Locations (1)

Retina Consultants of Texas Research Centers; 🇺🇸 Houston, Texas, United States