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NCT04831177

Thin-Flap Laser in Situ Keratomileusis Associated Dry Eye

Completed NA Last updated 6 April 2021
What this trial tests

NA trial testing Laser in situ keratomileusis in Myopic LASIK Candidates With Spherical Equivalent up to - 10 Diopters in 55 participants. Completed in 1 September 2020.

Timeline
1 June 2019
Primary endpoint
1 September 2020
1 September 2020

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment55
Start date1 June 2019
Primary completion1 September 2020
Estimated completion1 September 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

18 and older, any sex, with Myopic LASIK Candidates With Spherical Equivalent up to - 10 Diopters. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Laser in situ keratomileusis (LASIK) eye surgery continues to be the most common refractive procedure used to correct different forms of ametropia. Although the introduction of femtosecond technology has markedly reduced the incidence of intraoperative flap complications and allowed a better control on flap parameters, dry eye remains one of the most challenging postoperative complications.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Assiut University trials

Trials by the same sponsor.

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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/NCT04831177.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing