A Study of a Novel Scheimpflug Device in Diagnosing Keratoconus

NCT06119321 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2024-11-04

No results posted yet for this study

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.

Conditions

  • Scansys
  • Pentacam
  • Corvis ST
  • Keratoconus
  • Subclinical Keratoconus

Interventions

OTHER

Pentacam, Corvis ST and Scansys

morphological and biomechanical parameters of corneal were obtain by Scansys, Pentacam and Corvis ST

Sponsors & Collaborators

  • Tianjin Eye Hospital

    lead OTHER

Principal Investigators

  • Yan Wang, Prof · Tianjin Eye Hospital

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-04
Primary Completion
2023-11-01
Completion
2024-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06119321 on ClinicalTrials.gov