33 Participants Needed

To Study the Effects of Refractive Surgery on OCT Measurements in the Eye

Recruiting at 1 trial location
PR
TF
PP
TA
Overseen ByTolulope A Fashina, MD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Nebraska
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

Trial Summary

What is the purpose of this trial?

Corrective eye surgeries, such as Lasik, are widely used to correct focusing problems such as myopia, or nearsightedness. Often these patients develop other conditions like myopic maculopathy or glaucoma which require monitoring with optical coherence tomography (OCT). Since OCT is a light-based test and changes the refractive status of the eye (in the cornea or the lens), it can potentially affect the results of the OCT measurements but has not been sufficiently studied. This pilot study aims at studying the potential change in OCT parameters in the eye after undergoing such surgery.

Research Team

PP

Pukhraj P Rishi, MBBS

Principal Investigator

University of Nebraska

Eligibility Criteria

Inclusion Criteria

Patients undergoing refractive surgery
For patients undergoing bilateral eye surgery, the one with higher degree of ametropia will be included.

Treatment Details

Interventions

  • Optical coherence tomography
  • Refractive Surgery
Participant Groups
1Treatment groups
Experimental Treatment
Group I: Ocular parametersExperimental Treatment1 Intervention
Patients aged 19 years or more who are scheduled to undergo refractive surgery will be included in the study. OCT will be performed at baseline (before surgery), 1 day after surgery and 1 week after surgery. Each patient will be tested 3 times.

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Nebraska

Lead Sponsor

Trials
563
Recruited
1,147,000+