iCare ST500 Clinical Trial

Conditions: Intraocular Pressure

Sex: All

Ages: 18 Years – N/A

Healthy volunteers: 1

Phase: NA

Enrollment: 150

Sponsor: Icare Finland Oy

Summary

Clinical validation of iCare ST500 tonometer per ANSI Z80.10:2014 standard

Eligibility Criteria

Inclusion Criteria:Patients at least 18 years oldExclusion Criteria:Subjects with only one functional eyeSubjects having poor or eccentric fixation in the study eye(s)High corneal astigmatism >3D in the study eye(s)Central corneal scarringHistory of prior incisional glaucoma surgery or corneal surgery, including corneal refractive laser surgery in the study eye(s)MicrophthalmosBuphthalmosContact lens use within one week of continuous wear and within one hour if lens is worn occasionallyDry eyes (clinically significant)Lid squeezers - blepharospasmNystagmusKeratoconusAny other corneal or conjunctival pathology or infection relevant to this studyCentral corneal thickness greater than 600 μm or less than 500 μm in the study eye(s)Cataract Extraction within last 2 months in the study eye(s)

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05742009). StuddyBuddy aggregates publicly available trial information.