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Self/ Home measurement of Intra-ocular pressure by Icare Home Device as compared to professional tonometry

Not Applicable
Conditions
Health Condition 1: H401- Open-angle glaucomaHealth Condition 2: H408- Other glaucomaHealth Condition 3: H402- Primary angle-closure glaucoma
Registration Number
CTRI/2019/11/022125
Lead Sponsor
Isha Gupta
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patient diagnosed with primary or secondary glaucoma presenting with his/her caregiver, wherein both are willing to give informed written consent

Exclusion Criteria

1. Patients with any corneal pathology including corneal edema.

2. Best corrected near visual acuity of more than N.8 or far acuity of more than 6/9.

3. Patients with learning disability.

4. Patients with motor disability/neurological disease â?? ocular and systemic.

(Parkinsonâ??s disease, muscular dystrophies, hand tremors, myasthenia gravis)

5. Patients who cannot be examined on slit lamp due to postural deformities.

6. Patients with any macular pathology.

7. Eye with any active infection or inflammation (acute red eye).

8. History of or any ocular surgery less than 6 months before the date of recruitment.

9. History of any corneal surgery irrespective of time since surgery.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Inter-device agreement between Icare Home(TA022) and Goldmann applanation tonometer. <br/ ><br>2. Inter-device agreement between Icare Home(TA022) and Icare (ic100) tonometer. <br/ ><br>3. Inter-user agreement of Icare Home(TA022) between patient and caregiverTimepoint: May 2019
Secondary Outcome Measures
NameTimeMethod
Ease of use of Icare home Device by patients and their caregiversTimepoint: On the day of enrollment
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