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Reliability of Pachymetry Measurement With FD-oCT, ORA, Confoscan 4 and Ultrasound

NCT00838422 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2009-02-06

No results posted yet for this study

Summary

The purpose of this study is to assess the repeatability, reproducibility, and agreement of central corneal thickness measured by Fourier Domain Optical Coherence tomography (FD-OCT, OptoVue, USA) with anterior corneal module, 20MHz ultrasound pachymetry equipped with Ocular response analyzer (ORA, Reichert Ophthalmic Instruments, USA) and 10MHz Ultrasound Pachymetry (USP).

Conditions

  • Keratitis

Sponsors & Collaborators

  • Far Eastern Memorial Hospital

    lead OTHER

Principal Investigators

  • Shu-Wen Chang, MD · Far Eastern Memorial Hospital

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2009-01-31
Completion
2009-06-30

Countries

  • Taiwan

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 NCT00838422 on ClinicalTrials.gov