Corneal Incision vs. Toric Lens for Cataract Surgery Astigmatism
Corneal Incision
+ Toric Intraocular
Services Research Study
Summary
Study start date: October 1, 2020
Actual date on which the first participant was enrolled.The study aims to compare two different methods used during cataract surgery to address astigmatism, a common issue where the eye does not focus light evenly on the retina. These methods include making small cuts on the edge of the cornea, known as limbal relaxing incisions (LRIs), and using a special type of lens called a toric intraocular lens (IOL). The focus is on understanding which of these techniques is more beneficial for patients who have astigmatism before surgery, helping them achieve better vision outcomes. Participants will undergo cataract surgery using one of the two methods. Those receiving LRIs will have small incisions made on the cornea to reshape it, while others will have a toric IOL implanted to correct the astigmatism. The study will evaluate how well each method corrects the patient's vision and reduces astigmatism. The results will help determine the most effective approach for improving vision quality in cataract patients with pre-existing astigmatism.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.368 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 35 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location