Measurement of Eye pressure through new instrument Icare HOME (TA022) tonometer among normal and Glaucoma patients.
- Conditions
- Health Condition 1: null- Normals and glaucoma patients
- Registration Number
- CTRI/2018/07/014818
- Lead Sponsor
- Icare Finland Oy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1)Patients with or without glaucoma will be included in study
2)Patients with any intraocular pressure will be included in the study
1)Uncorrected Near Visual Acuity (UCNVA) of 20/200 (binocular)
2)Participants with only one functional eye
3)Participants having poor or eccentric fixation in the study eye
4)Hearing impaired to the extent that the individual cannot hear and converse with others without an assistive aid and/or sign language
5)All corneal pathologies
6)Disabling arthritis or limited motor coordination limiting self-handling of the Icare Home tonometer
7)Inability to demonstrate proficiency with Icare Home tonometer after training and failure to complete certification procedures
8)Cataract Extraction within last 2 months in study eye
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraocular pressure in mmHgTimepoint: may, 2019
- Secondary Outcome Measures
Name Time Method patient comfort scaleTimepoint: may, 2019