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Measuring Corneal Parameters

RecruitingNA

Sponsor: Icare Finland Oy

Conditions: Corneal Parameters

Interventions: Investigational device, Comparator device

Countries: Germany

The aim of this clinical investigation is to assess the feasibility of the investigational device for measuring corneal parameters of the human eye.

Eligibility overview

Sex: ALL

Age: 18 Years to —

Healthy volunteers: Yes

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

1\. Age ≥ 18 years

Exclusion Criteria:

1. Subjects with only one functional eye
2. Subjects having poor or eccentric fixation in the study eye(s)
3. Central corneal scarring (that might affect the measurement result)
4. Microphthalmos
5. Buphthalmos
6. Contact lens use (12 hours prior to measurements)
7. Severe dry eyes
8. Lid squeezers - blepharospasm
9. Nystagmus
10. Any other corneal or conjunctival pathology or condition that prevents CCT measurements

Locations (1)

Bonn, North Rhine-Westphalia, Germany