Health Condition 1: H259- Unspecified age-related cataract
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 Pupil size = 4 mm post pharmacological dilatation as study subjects and a control group with normal pupil size >4mm 2 All grades of Cataract. 3 Patients willing to participate in the study.
Exclusion criteria
Exclusion criteria: 1 Active iritis in the past 3 months. 2 Current Ocular inflammation. 3 Posterior synechiae > 1 clock hour. 4 Advanced Glaucoma with macular threat. 5 Specular microscopy count 6 Subluxated lens / Traumatic cataract. 7 Corneal disorders like corneal opacity, degenerations and dystrophies and congenital anterior segment anomalies. 8 History of Previous retinal surgeries. 9 Posterior segment anomalies affecting the visual acuity. 10 Age 11 Patients unwilling to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To measure pre-operative, intra-operative and post-operative pupil size and to record intra-operative and post-operative complications if any, with each method.Timepoint: Patient will be followed up on Day 1, Day 7 and 1 month. Pre-operative pupil size will be measured post-mydriasis before the surgery Intra-operative pupil size will be measured a Before entering the anterior chamber b Post OVD injection c Post mechanical dilatation d End of the surgical procedure Post-operative pupil size will be measured on Day 7 and 1 month | — |
Secondary
| Measure | Time frame |
|---|---|
| 1 To record the Visual Acuity before and after the surgery. 2 To measure pre-operative and post-operative endothelial cell count using specular microscopy. 3 To compare the above parameters recorded in each method used. Timepoint: Visual acuity will be recorded pre-operative and post-operatively Day 7 and 1 month. Specular microscopy will be recorded pre-operatively and 1 month post-operatively. | — |
Countries
India
Contacts
Sankara Eye Hospital