Glaucoma screening using smartphones

Phase 4

• Conditions: Health Condition 1: H409- Unspecified glaucoma

• Registration Number: CTRI/2021/01/030724
• Lead Sponsor: Dr Arvind kumar morya

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.Patients in the age group of 20 â?? 70 years.

2.Patients willing to give written informed consent.

Exclusion Criteria

1.Patients who are not unable to understand the procedure.

2.Patients having the retinal pathologies.

3.Patients who have vision BCVA less than 6/60.

4.Patients having contagious communicable disease.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary objectives of this study are Virtual Reality based Visual Field Testing and Anterior segment imaging based IntraOcular Pressure (IOP) estimation and Visual Acuity assessment.Timepoint: OPD Day 1 and OPD Day 3

Secondary Outcome Measures

Name	Time	Method
a secondary objective is to validate the use of a smartphone based Visual Acuity Test without any ophthalmic apparatus thus paving the way to a prospective tele-ophthalmology application.Timepoint: 18 MONTHS