Measuring Corneal Parameters

Starting soon · Not applicable

Conditions studied: Corneal Parameters

In brief

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

Key facts

Study ID

NCT07629232

Run by

Icare Finland Oy

People needed

50

Starts

2026-05-27

Expected to finish

2026-07-31

Last updated by the study team

2026-06-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Age ≥ 18 years

You may not qualify if…

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

Where it is running

• Universitäts-Augenklinik Bonn — Bonn, North Rhine-Westphalia, Germany

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.