Improvement of refractive outcomes in myopic regression after Laser in Situ Keratomileusis using timolol: A randomised clinical trial
Not Applicable
- Conditions
- Regression after lasik surgery.Myopia
- Registration Number
- IRCT138706271258N1
- Lead Sponsor
- Tehran University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Having undergone Lasik surgery, both eyes have had at least -0.5 D return
Exclusion criteria: Incidence of complications during the surgery, presence of background diseases such as glaucoma, heart failure, digestive problems, cancer, favism, myasthenia gravis, or asthma
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Refractive error. Timepoint: before intervention; 2 months and 6 months after intervention. Method of measurement: auto refractive, objective refractive, subjective refractive.
- Secondary Outcome Measures
Name Time Method