Myopic Regression
Conditions
Brief summary
In this randomized controlled clinical trial, we compare the effects of timolol versus placebo for treatment of myopic regression after LASIK
Interventions
artificial tear twice a day
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with myopic regression equal or more than 0.5 D with minimum age of 20 years, * cylinder ≤ -1.00 D, * corrected distance visual acuity (CDVA) of at least 20/40 were included.
Exclusion criteria
* Patients with a history of previous ocular surgery, * keratoconus or any ectatic corneal disorder, * keratoconus suspect by topography, * preoperative corneal opacity, * any corneal dystrophies, * presence of pterygium, * retinal disorders, * collagen vascular disorders, * diabetes mellitus, * glaucoma, * cataract, * pregnancy, * breast feeding * systemic corticosteroid therapy were excluded.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Spherical Equivalent | spherical equivalent at month 6 | Effect of timolol use in timolol group will be compared with placebo group at month 6. Moreover, the changes of intragroup spherical equivalent will be assessed in both group 6 months after timolol application. |
Countries
Iran