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

NCT ID: NCT02445313

Last Updated: 2019-02-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-06-30

Study Completion Date

2019-02-12

Brief Summary

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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.

Detailed Description

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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).

Conditions

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Age-related Macular Degeneration (AMD)

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Control

Normal, healthy participants

Nidek MP-3

Intervention Type DEVICE

Nidek MP-3 device to be used to take images which will allow measurement of GA in patients with AMD

AMD

Age-related Macular Degeneration participants

Nidek MP-3

Intervention Type DEVICE

Nidek MP-3 device to be used to take images which will allow measurement of GA in patients with AMD

Interventions

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Nidek MP-3

Nidek MP-3 device to be used to take images which will allow measurement of GA in patients with AMD

Intervention Type DEVICE

Eligibility Criteria

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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.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Doheny Image Reading Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Srinivas Sadda

Role: PRINCIPAL_INVESTIGATOR

Doheny Eye Institute

Locations

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Doheny Eye Centers UCLA

Pasadena, California, United States

Site Status

Countries

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United States

Other Identifiers

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NIDEKMP3

Identifier Type: -

Identifier Source: org_study_id

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