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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03890718
Other study ID # ShaheidBU
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date March 30, 2017
Est. completion date December 15, 2023

Study information

Verified date January 2022
Source Shahid Beheshti University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To our knowledge, this study is one of the first to compare the visual results of non-topography-guided and topography-guided photorefractive keratectomy (PRK) applying sequential and simultaneous corneal cross-linking (CXL) treatment for keratoconus. Considering recent advances in cross-linking and imaging in keratoconus, the outcomes of this study can lead us to several non-invasive algorithm management options.


Description:

Interventional and comparative prospective study: Sixty-nine eyes (38 patients) suffering from keratoconus (stages 1-2 Amsler-Krumeich classification) were divided into four groups. The four groups underwent topography- and non-topography-guided PRK with sequential and simultaneous CXL. The main outcome measures were pre- and postoperative uncorrected distance visual acuity (UDVA), best corrected distance visual acuity (CDVA), manifest refraction, contrast sensitivity, and keratometry.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 38
Est. completion date December 15, 2023
Est. primary completion date September 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 34 Years to 41 Years
Eligibility Inclusion criteria - age 34 (range from 34 to 41) - stable corneal topography and refraction for at least six months - estimated residual bed thickness of >410 µm Exclusion - presence of macular or retinal disease, - dry eye - history of recurrent corneal erosions - anterior segment abnormalities - unstable refractive error - post-surgically residual stromal bed thickness of under 350 mm - autoimmune disease - collagen vascular disease - immunosuppressive therapy or current use of systemic corticosteroids - diabetes mellitus - pregnancy - lactation

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Photorefractive keratectomy in mile keratoconus
Topo-guided photorefractive keratectomy will be performed using an excimer laser (Allegretto Wave Topolyzer, Alcon, Inc.) with a 6 mm optical area and a transition area of 2 mm in all eyes. At that point, the partial topography-guided photorefractive keratectomy laser treatment will be finished. The arrangement will be to treat 70% of the cylindrical and spherical part to not surpass 50µm of stromal expulsion. The estimation of 50µm as the most extreme removal depth recommended by Kanellopoulos in Athens protocol will be chosen

Locations

Country Name City State
Iran, Islamic Republic of Farideh Doroodgar Tehran

Sponsors (1)

Lead Sponsor Collaborator
Shahid Beheshti University

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Other Aberrometry properties by iTrace Ray-tracing aberrometry Optical aberrations are a major cause for poor quality of vision. It occurs when light from one point, after transmission through an optical system, does not converge to or diverge from a single point. Any deviation of the optical system from paraxial optics results in aberrations. In the eye, the various refracting surfaces like tear film, cornea and lens are primarily responsible for inducing ocular aberrations. The difference in shape of the wave-front entering the eye and that exiting the eye defines the type of aberration. The ocular aberrations are classified into lower order aberration (LOA) (zero order- piston; first order- horizontal and vertical tilt; second order- spherical defocus and astigmatism) and higher order aberrations (HOA) (third order - coma and trefoil; fourth order - quatrefoil, secondary astigmatism and spherical aberrations; fifth order - pentafoil; sixth order - hexafoil). 3 year
Primary visual acuity Visual acuity (VA) commonly refers to the clarity of vision 3 months
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