Comparation of Different Devices to Measure Corneal Thickness

Sponsor
Technische Universität Dresden (Other)
Overall Status
Unknown status
CT.gov ID
NCT01251705
Collaborator
(none)
70
1
3
23.2

Study Details

Study Description

Brief Summary

Comparison of different methods for measuring peoples corneal thickness

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Volunteers with healthy corneas will be measured by different instruments to detect their corneal thickness. First interindividual difference between the instruments will be reviewed. People will be measured again two times on two different days to examine an interindividual difference in all instruments.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    70 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Comparation of Different Devices to Measure Corneal Thickness
    Study Start Date :
    Nov 1, 2010
    Anticipated Primary Completion Date :
    Dec 1, 2010
    Anticipated Study Completion Date :
    Feb 1, 2011

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years and Older
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      • healthy cornea
      Exclusion Criteria:
      • myopia or astigmatism over 1,5 dpt

      • corneal surgery

      • acute ocular inflammation

      • lost of vision

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Departement of Ophthalmology Dresden Saxonia Germany 01307

      Sponsors and Collaborators

      • Technische Universität Dresden

      Investigators

      • Principal Investigator: Haustein, Doctor med., Departement of Ophthalmology University of Dresden

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT01251705
      Other Study ID Numbers:
      • CompCornea
      First Posted:
      Dec 2, 2010
      Last Update Posted:
      Dec 2, 2010
      Last Verified:
      Dec 1, 2010

      Study Results

      No Results Posted as of Dec 2, 2010