Ocular Imaging Study Using Advanced OCT

NCT02827071 | Terminated

• 1 other identifier: JSEI Nidek Advanced OCT
• Study Type: observational
• Target: 150
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to evaluate this AngioScan angiography software on patients with various retinal vascular disorders. The advanced OCT instrument is an FDA approved clinically used camera, but the AngioScan angiography software is not FDA approved. Investigators would like to know if this imaging device and software can improve the quality of images and visualization of imaged tissues and whether they are useful in the diagnosis and treatment of eye diseases. Images collected in this study may be compared to other images collected as part of standard of care on the same patient (OCT, FA, AF, Fundus).

Conditions

Retinal Vascular Disorder; Macular Degeneration

Outcome Measures

Primary Outcomes (1)

• Retinal vascular abnormalities imaged by OCT Angiography and en face analysis of macular disorders

  2 years

Study Arms (1)

Retina abnormalities

Subjects with various retina vascular disorders

Eligibility Criteria

• Age: 18 Years - 115 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Subjects with retinal vascular abnormalities

You may qualify if:

• Any patient with abnormal retinal findings as determined by investigators.

You may not qualify if:

• Those suffering from head, neck or other injury which makes them unable to position themselves in head restraint for imaging.
• Participants who are unable to maintain retinal fixation on a specified target.
• Participants unable to achieve sufficient pupil dilation and alignment stability for imaging to take place.
• Patients with media opacity which preclude high quality imaging.

Sponsors & Collaborators

• University of California, Los Angeles: lead

Study Sites (1)

Stein Eye Institute/Geffen School of Medicine

Los Angeles, California, 90095, United States

Location

MeSH Terms

Conditions

Macular Degeneration

Condition Hierarchy (Ancestors)

Retinal Degeneration; Retinal Diseases; Eye Diseases

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 6, 2016
• First Posted: July 11, 2016
• Study Start: July 1, 2016
• Primary Completion: December 9, 2021
• Study Completion: December 9, 2021
• Last Updated: April 20, 2026

Record last verified: 2016-07

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)