MP3 (Microperimeter 3) Reproducibility in Healthy Subjects and Macular Patients

NCT ID: NCT02941406

Last Updated: 2016-10-21

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

UNKNOWN

Total Enrollment

22 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-07-31

Study Completion Date

2016-12-31

Brief Summary

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The aim of the present study is to investigate the reproducibility of the MP3 and to compare the results with conventional perimetry using the Octopus 101 in healthy subjects and patients with macular disease.

Detailed Description

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Conditions

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Macular Degeneration

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Healthy subjects

* Men and Women aged 18 and older
* Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant
* Normal ophthalmological findings unless the investigator considers an abnormality to be clinically irrelevant

No interventions assigned to this group

Age-related macular degeneration patients

* Men and Women aged 18 and older
* Presence of a macular disease (such as dry or exudative age-related macular degeneration, diabetic maculopathy, epiretinal membrane)

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Men and Women aged 18 and older
* Written informed consent
* Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant
* Normal ophthalmological findings unless the investigator considers an abnormality to be clinically irrelevant


* Men and Women aged 18 and older
* Written informed consent
* Presence of a macular disease (such as dry or exudative age-related macular degeneration, diabetic maculopathy, epiretinal membrane)

Any of the following will exclude a subject from the study:

* Any opacities (corneal scar, dense cataract) which interferes with the study relevant measurements
* Visual acuity \< 0.1 (Snellen)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Vienna Institute for Research in Ocular Surgery

OTHER

Sponsor Role lead

Responsible Party

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Prim. Prof. Dr. Oliver Findl, MBA

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Oliver Findl, MD, Prof.

Role: PRINCIPAL_INVESTIGATOR

Vienna Institute for Research in Ocular Surgery

Locations

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Hanusch-Krankenhaus

Vienna, Vienna, Austria

Site Status

Countries

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Austria

Other Identifiers

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MP3_REP

Identifier Type: -

Identifier Source: org_study_id

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