Data Collection With the P200TE and P200TxE
Not Applicable
Terminated
- Conditions
- Retinal Disease
- 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
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
- 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.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Retina Consultants of Texas Research Centers
🇺🇸Houston, Texas, United States
Retina Consultants of Texas Research Centers🇺🇸Houston, Texas, United States