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

Not Applicable

• Conditions: H40.1; H40.0; H40.2; Primary open-angle glaucoma; Glaucoma suspect; Primary angle-closure glaucoma

• Registration Number: DRKS00007654
• Lead Sponsor: niversitätsklinikum Münster

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-01-05
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

group A (glaucoma patients)

glaucoma damage

group B (non-glaucoma patients)

patients in ophthalmologic care without glaucoma

Exclusion Criteria

group A (glaucoma patients)

corneal blurring
pregnancy
lactation period

group B (non-glaucoma patients)

glaucoma damage
pregnacy
lactation period

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
patient satisfaction measured by a visual analog scale, using a questionnaire