To compare one photo taking device of the eye with another photo taking device of the eye in case of far sightedness.

Not Applicable

Not yet recruiting

• Conditions: Health Condition 1: H520- Hypermetropia

• Registration Number: CTRI/2023/05/052995
• Lead Sponsor: Meenakshi Sharma

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

1.Hypermetropes

2.IOL power between 24D- 28D

3.Age :45 years- 65 years

4.Patients opting for cataract surgeries with immature cataract

Exclusion Criteria

1.Myopes

2.IntraOcular Lens power <24D or >28D

3.Infective pathology

4.Acute intraocular trauma

5.Patients with poor media clarity due to corneal edema, dense cataracts,vitreous haemorrhage and asteroid hyalosis.

6.Pupil size less than 4mm

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the efficacy of the 2 imaging machines i.e. Anterion and AS OCT.Timepoint: The required data is collected at the same time when the patient sits for the test. <br/ ><br>But the comparison of results from the 2 machines is done towards the end of the study that is at the time of analysis of the results .

Secondary Outcome Measures

Name	Time	Method
To compare the time taken by each machine individually to give the results.Timepoint: The required data is received at the the time of the imaging on the 2 machines.