None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients aged 50 years and above Patients with hypermetropia Patients with short axial length and normal axial length Patients willing to participate in the study
Exclusion criteria
Exclusion criteria: Patients with myopia Patient with history of intraocular surgery penetrating trauma in the eye previous anterior segment laser treatment corneal disorders such as corneal endothelial dystrophy corneal opacity Patient with an aphakic or pseudophakic eye
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the sensitivity and specificity of AOD 750,ACA and ARA in detecting angle closure compared to gonioscopyTimepoint: at baseline 4 weeks 8weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess whether AOD 750 or ACA is a predictor for detecting of angle closure in hypermetropic patients with normal & short axial length when compared to gonioscopyTimepoint: baseline 4weeks 8weeks | — |
Countries
India
Contacts
Indra Gandhi Govt General Hospital Post Graduate Institution