TopQ Cut-off Determination Study For 3D-OCT 1 Maestro and 3D OCT-2000
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT02203981 |
Recruitment Status :
Completed
First Posted : July 30, 2014
Last Update Posted : October 23, 2014
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Condition or disease |
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Healthy |
Study Type : | Observational |
Actual Enrollment : | 12 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Official Title: | TopQ Cut-off Determination Study For 3D-OCT 1 Maestro and 3D OCT-2000 |
Study Start Date : | January 2014 |
Actual Primary Completion Date : | July 2014 |
Actual Study Completion Date : | August 2014 |
- Retinal Thickness [ Time Frame: Day 1 ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- No known ocular pathologies
Exclusion Criteria:
- Any known ocular pathologies

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02203981
United States, New Jersey | |
Topcon Medical Systems, Inc. | |
Oakland, New Jersey, United States, 07436 |
Principal Investigator: | Sunni Patel, PhD | Topcon Corporation |
Responsible Party: | Topcon Medical Systems, Inc. |
ClinicalTrials.gov Identifier: | NCT02203981 |
Other Study ID Numbers: |
TopQ_Maestro_OCT2000_001 |
First Posted: | July 30, 2014 Key Record Dates |
Last Update Posted: | October 23, 2014 |
Last Verified: | October 2014 |
normal Eyes |