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NCT05261685

Single-step Transepithelial PRK for Hyperopia

Completed NA Last updated 12 July 2022
What this trial tests

NA trial testing Single-step transepithelial PRK in Moderate Hyperopia in 30 participants. Completed in 15 December 2021.

Timeline
1 December 2019
Primary endpoint
15 December 2021
15 December 2021

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date1 December 2019
Primary completion15 December 2021
Estimated completion15 December 2021
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

18 and older, any sex, with Moderate Hyperopia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hyperopia is one of the commonest refractive errors encountered in ophthalmology practice. Laser in situ keratomileusis (LASIK) has been widely used to correct hyperopia especially with the advent of femtosecond laser technology allowing larger flap creation suitable for peripheral hyperopic ablations with resultant predictable, effective, and safe refractive outcomes. However, the encountered LASIK flap complications encouraged many surgeons to assess efficiency and safety of surface ablation techniques such as photorefractive keratectomy (PRK) to correct hyperopia.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Twelve-month outcomes of single-step transepithelial photorefractive keratectomy for moderate hyperopia and hyperopic astigmatism.
    Abdel-Radi M, Rateb M, Saleh MGA, Aly MOM. · · 2023 · cited 7× · PMID 36855211 · DOI 10.1186/s40662-023-00327-4

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Other trials of Single-step transepithelial PRK

Trials testing the same drug.

Other Assiut University trials

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05261685.

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