Status:
UNKNOWN
Defining the Operating Parameters for a Rebound-esthesiometer
Lead Sponsor:
Icare Finland Oy
Conditions:
Corneal Sensation Reduced
Corneal Dystrophy
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this study is to define the operating parameters for a new method to measure corneal sensitivity.
Detailed Description
Corneal sensitivity is the most important protective mechanism of the eye. Thus, measuring it at any given time gives important indicators of corneal physiology, especially in the diagnostics of corne...
Eligibility Criteria
Inclusion
- Age \>= 18
- Informed consent signed
Exclusion
- Signs of infectious or inflammatory disease of anterior eye at the time of presentation.
- During last two weeks, any of the following events or conditions occurred or was present: inflammatory or infectious ocular condition, surgical or other intervention or therapy, other abnormal ocular event.
- Unable to give informed consent.
- Directly or indirectly indicated vunerability.
Key Trial Info
Start Date :
August 1 2020
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2020
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT04384094
Start Date
August 1 2020
End Date
December 1 2020
Last Update
July 29 2020
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