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The aim of this clinical investigation is to assess the feasibility of the investigational device for measuring corneal parameters of the human eye.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Measurement with the investigational device | Experimental |
| |
| Measurement with Zeiss IOL Master 700 | Experimental |
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| Measurement with Heidelberg Anterion | Experimental |
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| Measurement with Nidek NT-530P | Experimental |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Investigational device | Device | Measurement of corneal parameters |
|
| Measure | Description | Time Frame |
|---|---|---|
| The primary objective of this study is to collect a comprehensive dataset of central corneal thickness (CCT) values to assess the performance of investigational device. | Through study completion, an average of 2 months |
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Inclusion Criteria:
1. Age ≥ 18 years
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Maximilian Pfau, Prof. | Contact | +4915164672802 | Maximilian.Pfau@ukbonn.de |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Universitäts-Augenklinik Bonn | Bonn | North Rhine-Westphalia | 53127 | Germany |
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| Comparator device | Device | Measurement of corneal parameters |
|