Self-measurement of intraocular pressure and using a rebound tonometer (iCare HOME)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00007654

Enrollment

200

Registered

2015-01-05

Start date

2015-01-07

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

H40.1 H40.0 H40.2

Interventions

Group 1: intraocular pressure measured by iCare HOME tonometry by the doctor (glaucoma & non-glaucoma patients) Group 2: intraocular pressure measured by iCare HOME tonometry by the patient (glaucoma

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: group A (glaucoma patients) glaucoma damage group B (non-glaucoma patients) patients in ophthalmologic care without glaucoma

Exclusion criteria

Exclusion criteria: group A (glaucoma patients) corneal blurring pregnancy lactation period group B (non-glaucoma patients) glaucoma damage pregnacy lactation period

Design outcomes

Primary

Measure	Time frame
intraocular pressure measured with iCare HOME (doctor and patient), iCare ONE (doctor and patient) and Goldmann applanation tonometry (only doctor). All togther 5 measurements	—

Secondary

Measure	Time frame
patient satisfaction measured by a visual analog scale, using a questionnaire	—

Countries

Germany

Contacts

Public ContactAndré Rosentreter

Universitätsklinikum Münster

andre.rosentreter@googlemail.com0251-83-56001

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026