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Measuring Geographic Atrophy in AMD Patients Using the Nidek MP-3 Microperimetry Device

D

Doheny Image Reading Center

Status

Completed

Conditions

Age-related Macular Degeneration (AMD)

Treatments

Device: Nidek MP-3

Study type

Observational

Funder types

Other

Identifiers

NCT02445313
NIDEKMP3

Details and patient eligibility

About

The investigators would like to know if different imaging devices can improve the quality of images and visualization of imaged tissues. Also, the investigators would like to find out whether these changes are useful in the diagnosis and treatment of eye diseases. Using images of previous participants will allow us to demonstrate the advancement of different technologies, as well be used to allow comparisons between current technologies.

Full description

To test the quality of images from the Nidek MP-3 device and to measure Geographic Atrophy (GA) in patients with Age-related Macular Degeneration (AMD).

Enrollment

100 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Normal, healthy participants and patients with AMD

Exclusion criteria

  1. Those suffering from head, neck or other injury which makes them unable to position themselves in head restraint for imaging
  2. Participants who are unable to maintain retinal fixation on a specified target
  3. Participants unable to achieve sufficient pupil dilation and alignment stability for imaging to take place
  4. Patients with media opacity which preclude high quality imaging will be excluded.
  5. Exclusion criteria include vulnerable patients; patients under 18, pregnant, economically and educationally disadvantaged, decision impaired, or homeless people. We exclude pregnant women because pregnancy often can alter eye anatomy.

Trial design

100 participants in 2 patient groups

Control
Description:
Normal, healthy participants
Treatment:
Device: Nidek MP-3
AMD
Description:
Age-related Macular Degeneration participants
Treatment:
Device: Nidek MP-3

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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