Health Condition 1: null- Patients with cataract
Conditions
Interventions
Intervention1: Toric IOL implantation: The patients were implanted either plate haptic toric IOL (AT Torbi, Zeiss)(Group 1) or loop haptic toric IOL (Acrysof)(Group 2)
Control Intervention1: Group 1:
Sponsors
Government Medical College and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Patients with cataract associated with preoperative regular corneal astigmatism between 1-5 D
Exclusion criteria
Exclusion criteria: Patients with irregular astigmatism, corneal dystrophy, tear-film instability, pupillary abnormalities, glaucoma, uveitis, retinal diseases, optic atrophy, or neuro-ophthalmic disease were excluded. Patients developing intra-operative complications like posterior capsule rent or extension of capsulorhexis or zonular dialysis were also excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Uncorrected visual acuity, Best corrected visual acuity (BCVA), Keratometry, IOL position after full mydriasis by masked observer on slit lamp biomicroscopeTimepoint: Postoperatively at 1 week, 1 month and 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| A note of complications such as persistent corneal edema, pupillary block, retinal detachment, endophthalmitis and/ or need for neodymium:YAG capsulotomyTimepoint: Postoperatively at 1 week, 1 month and 3 months | — |
Countries
India
Contacts
Public ContactRakesh Kumar Bansal
Government Medical College and Hospital Chandigarh
Outcome results
None listed