iCare IC1000 Alignment Study

Not Applicable

Recruiting

• Conditions: Intraocular Pressure

• Registration Number: NCT07022054
• Lead Sponsor: Icare Finland Oy

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2025-05-22
• Study First Submitted: 2025-05-22
• Status Verified: 2025-06
• Study First Submitted QC: 2025-06-13
• Last Update Submitted: 2025-06-13
• Study First Posted: 2025-06-15
• Last Update Posted: 2025-06-15
• Primary Completion: 2025-07
• Study Completion: 2025-07

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 100

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

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Primary Objective	Through study completion, an average of 2 months	Number of participants with successful intraocular pressure (IOP) measurements using the alignment feature of the iCare IC1000 tonometer during a single clinic visit.

Trial Locations

Locations (1)

Clear Vue Laser Eye Center; 🇺🇸 Lake Worth, Florida, United States