Measuring Corneal Parameters

Feasibility Study - Measuring Corneal Parameters

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07629232

Enrollment

Registered

2026-06-05

Start date

2026-06-01

Completion date

2026-09-30

Last updated

2026-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corneal Parameters

Brief summary

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

Interventions

DEVICEInvestigational device

Measurement of corneal parameters

DEVICEComparator device

Measurement of corneal parameters

Study design

Allocation

NON_RANDOMIZED

Intervention model

SEQUENTIAL

Primary purpose

DEVICE_FEASIBILITY

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame
The primary objective of this study is to collect a comprehensive dataset of central corneal thickness (CCT) values to assess the performance of investigational device.	Through study completion, an average of 2 months

Countries

Germany

Contacts

CONTACTMaximilian Pfau, Prof.

Maximilian.Pfau@ukbonn.de+4915164672802

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 21, 2026