Comparison of Ultrasonic Pachymetry With Orbscan in Corneal Haze

Sponsor
Baskent University (Other)
Overall Status
Completed
CT.gov ID
NCT00439114
Collaborator
(none)
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Study Details

Study Description

Brief Summary

This study is planned to compare the results of ultrasonic and Orbscan pachymetry in corneal haze not related to surgery. Corneal haze is graded with slit-lamp by a single examiner. Ultrasonic and Orbscan II pachymetry measurements are obtained. Paired t and Kruskal-Wallis tests are used to evaluate the difference between ultrasonic and Orbscan pachymetry measurements. Correlation of the two methods and haze grade is determined with Kendall's tau-b correlation analysis.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    We planned this study to compare the results of ultrasonic and Orbscan pachymetry in corneal haze not related to surgery. In this institutional based, prospective, controlled clinical trial subjects with corneal haze not related to surgery are included. Normal eyes are used as control group to calculate the customized acoustic factor. Corneal haze is graded with slit-lamp by a single examiner. Ultrasonic and Orbscan II pachymetry measurements are obtained by one technician each masked to the other measurement. Paired t and Kruskal-Wallis tests are used to evaluate the difference between ultrasonic and Orbscan pachymetry measurements. Correlation of the two methods and haze grade is determined with Kendall's tau-b correlation analysis. According to the results of the study, we will determine which method is accurate in subjects with corneal haze.

    Study Design

    Study Type:
    Observational
    Observational Model:
    Defined Population
    Time Perspective:
    Other
    Official Title:
    Comparison of Ultrasonic Pachymetry With Orbscan in Corneal Haze
    Study Start Date :
    Jul 1, 2005
    Study Completion Date :
    Jun 1, 2006

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 71 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      • Patients with significant corneal haze on slit-lamp are included in the study group. 50 eyes of 50 age-matched patients with normal eye and clear cornea are included in the control group. Only one eye of each subject is included.
      Exclusion Criteria:
      • Exclusion criteria to participate in the study are previous ocular surgery, history of contact lens use, glaucoma, and topical ocular medication use, excluding artificial tears.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Baskent University, Faculty of Medicine, Adana Hospital Adana Turkey 01250

      Sponsors and Collaborators

      • Baskent University

      Investigators

      • Principal Investigator: Rana Altan-Yaycioglu, M.D., Baskent University, Faculty of Medicine, Department of Ophthalmology

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00439114
      Other Study ID Numbers:
      • KA05/207
      First Posted:
      Feb 23, 2007
      Last Update Posted:
      Feb 23, 2007
      Last Verified:
      Feb 1, 2007
      Keywords provided by , ,
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Feb 23, 2007