Status:
COMPLETED
Quick Measure Study for iCare ST500 and iCare IC200
Lead Sponsor:
Icare Finland Oy
Conditions:
Intraocular Pressure
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of this clinical study is to compare the agreement and precision of the intraocular pressure (IOP) results measured with the Quick Measure feature of iCare ST500 and iCare IC200 tonometers wit...
Eligibility Criteria
Inclusion
- 1\. Age ≥ 18 years
Exclusion
- Subjects with only one functional eye
- Subjects having poor or eccentric fixation in the study eye
- High corneal astigmatism \>3D in the study eye
- Central corneal scarring
- History of prior incisional glaucoma surgery or corneal surgery, including corneal refractive laser surgery in the study eye
- Microphthalmos
- Buphthalmos
- Contact lens use within one week of continuous wear and within one hour if lens is worn occasionally
- Dry eyes (clinically significant)
- Lid squeezers - blepharospasm
- Nystagmus
- Keratoconus
- Any other corneal or conjunctival pathology or infection relevant to this study
- Central corneal thickness greater than 600 μm or less than 500 μm in the study eye
- Cataract Extraction within last 2 months in the study eye
Key Trial Info
Start Date :
August 28 2025
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 3 2025
Estimated Enrollment :
122 Patients enrolled
Trial Details
Trial ID
NCT07156630
Start Date
August 28 2025
End Date
December 3 2025
Last Update
December 11 2025
Active Locations (1)
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1
NVision Clinical Research LLC
Torrance, California, United States, 90505