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Comparation of Different Devices to Measure Corneal Thickness

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified December 2010 by Technische Universität Dresden.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01251705
First Posted: December 2, 2010
Last Update Posted: December 2, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Technische Universität Dresden
  Purpose
Comparison of different methods for measuring peoples corneal thickness

Condition
Corneal Thickness

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Comparation of Different Devices to Measure Corneal Thickness

Further study details as provided by Technische Universität Dresden:

Estimated Enrollment: 70
Study Start Date: November 2010
Estimated Study Completion Date: February 2011
Estimated Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)
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.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
volunteers without corneal disease
Criteria

Inclusion Criteria:

  • healthy cornea

Exclusion Criteria:

  • myopia or astigmatism over 1,5 dpt
  • corneal surgery
  • acute ocular inflammation
  • lost of vision
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01251705


Contacts
Contact: Haustein, Doctor med. 0049351458 ext 3381 Michael.Haustein@uniklinikum-dresden.de
Contact: Wozniak 0049351458 ext 3381 Kathleen.Wozniak@uniklinikum-dresden.de

Locations
Germany
Departement of Ophthalmology Recruiting
Dresden, Saxonia, Germany, 01307
Contact: Haustein, Doctor med.    0049351458 ext 3381    Michael.Haustein@uniklinikum-dresden.de   
Contact: Wozniak    0049351458 ext 3381    Kathleen.Wozniak@uniklinikum-dresden.de   
Principal Investigator: Haustein, Doctor med.         
Sub-Investigator: Wozniak         
Sponsors and Collaborators
Technische Universität Dresden
Investigators
Principal Investigator: Haustein, Doctor med. Departement of Ophthalmology University of Dresden
  More Information

Responsible Party: L.E. Pillunat, University of Dresden
ClinicalTrials.gov Identifier: NCT01251705     History of Changes
Other Study ID Numbers: CompCornea
First Submitted: December 1, 2010
First Posted: December 2, 2010
Last Update Posted: December 2, 2010
Last Verified: December 2010

Keywords provided by Technische Universität Dresden:
Cornea
SL OCT
Spectral OCT Cornea modul
ultrasound pachymetry
Pentacam