Find out the Visual outcome of Phakic Intraocular Lens for the correction of Nearsightedness

A Study on Efficacy and Visual outcome of Posterior chamber Phakic Intra-ocular lens in High Myopia - Phakic IOL, Myopia

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2018/09/015651

Enrollment

Registered

2018-09-07

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- High Myopic Patients

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age >21 years 2. Stable refraction 3. Patients with myopia >-6.00D 4. Iridocorneal angle > 30 degree 5. Anterior chamber depth >2.7mm 6. Endothelial cell count > 2500 cells/sq.mm 7. Central corneal thickness >0.400 mm

Exclusion criteria

Exclusion criteria: 1. Age 2. Unstable refraction 3. Hyperopia 4. AC depth 5. Iridocorneal angle 6. Endothelial cell count 7. Central corneal thickness 8. Any Lens Changes 9.Any Retinal degeneration which cause Impaired vision 10.Any Inflammatory Pathologies of Eye 11.Any Previous Ocular Surgeries

Design outcomes

Primary

Measure	Time frame
1. Improvement in Best corrected visual acuity 2.Anterior chamber depth 3.Iridocorneal angle 4.Endothelial count 6.Central corneal thickness Timepoint: Post Op 1st Week 2nd Week 4th week 3rd Month and 6th Month	—

Secondary

Measure	Time frame
1.Intra Ocular Pressure 2.RIL Vaulting between Natural Lens and Phakic IOL 3.Any Other Adverse EventsTimepoint: Post Op 1st Week 2nd Week 4th week 3rd Month and 6th Month	—

Countries

India

Contacts

Public ContactProf Dr ANANDABABU M

Professor- Ophthalmology

anandcornea@yahoo.com9841183214

Outcome results