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Effect of Timolol on Refractive Outcomes in Eyes With Myopic Regression After LASIK: a Randomized Clinical Trial

Effect of Timolol on Refractive Outcomes in Eyes With Myopic Regression After Laser in Situ Keratomileusis: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01506635
Enrollment
45
Registered
2012-01-10
Start date
2010-03-31
Completion date
2010-12-31
Last updated
2012-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopic Regression

Brief summary

In this randomized controlled clinical trial, we compare the effects of timolol versus placebo for treatment of myopic regression after LASIK

Interventions

DRUGTimolol
DRUGPlacebo

artificial tear twice a day

Sponsors

Shahid Beheshti University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Spherical Equivalentspherical equivalent at month 6Effect 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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026