iCare IC1000 Alignment Study

Icare

Status: Enrolling

Conditions: Intraocular Pressure

Treatments: Device: iCare IC1000 measurement

Study type: Interventional

Funder types: Industry

Identifiers

NCT07022054

TA032-168

Details and patient eligibility

About

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

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

100 participants in 1 patient group

Measurement of IOP Values

Experimental group

Treatment:

Device: iCare IC1000 measurement