Status:

ACTIVE_NOT_RECRUITING

A Study of a Novel Scheimpflug Device in Diagnosing Keratoconus

Lead Sponsor:

Tianjin Eye Hospital

Conditions:

Scansys

Pentacam

Eligibility:

All Genders

Brief Summary

Comparison of the screening and diagnosis ability of the novel Scheimpflug-based tomography device (Scansys) with Pentacam and the Scheimpflug-based biomechanics device (Corvis ST) for keratoconus.

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Best corrected visual acuity (BCVA) ≥ 20/20;
  • No other eye diseases except myopia and astigmatism;
  • The cornea was transparent, and there was no cloud or pannus;
  • Exclusion Criteria:
  • The presence of ocular diseases other than myopia and keratoconus;
  • Ocular trauma;
  • Previous ocular surgery;
  • Patients were required to stop wearing soft contact lenses for at least 2 weeks and rigid contact lenses for at least 4 weeks before examination;
  • Pregnant and lactating women;

Exclusion

    Key Trial Info

    Start Date :

    May 4 2023

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    December 31 2024

    Estimated Enrollment :

    200 Patients enrolled

    Trial Details

    Trial ID

    NCT06119321

    Start Date

    May 4 2023

    End Date

    December 31 2024

    Last Update

    November 4 2024

    Active Locations (1)

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    Tiajin Eye Hospital

    Tianjin, Tianjin Municipality, China