Purpose

The primary objective of this study is to evaluate the performance of the alignment feature of iCare IC1000 tonometer.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  1. Age ≥ 18 years

Exclusion Criteria

  1. Subjects with only one functional eye 2. Central corneal scarring 3. Microphthalmos 4. Buphthalmos 5. Contact lens use during measurement or hard lenses 24h prior to measurement 6. Dry eyes (clinically significant) 7. Nystagmus 8. Keratoconus 9. Any other corneal or conjunctival pathology or infection relevant to this study 10. Coloboma or other pupil deformation

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Other
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Measurement of IOP Values
  • Device: iCare IC1000 measurement
    Measurement of intraocular pressure with iCare IC1000

Recruiting Locations

Clear Vue Laser Eye Center
Lake Worth, Florida 33467
Contact:
Monique Barbour, MD, Dr.
561-906-7292
dr.moniquebarbour@gmail.com

More Details

NCT ID
NCT07022054
Status
Recruiting
Sponsor
Icare Finland Oy

Study Contact

Monique Barbour, MD, Dr.
561-906-7292
dr.moniquebarbour@gmail.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.