Comparation of Different Devices to Measure Corneal Thickness

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2010 by Technische Universität Dresden.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Technische Universität Dresden
ClinicalTrials.gov Identifier:
NCT01251705
First received: December 1, 2010
Last updated: NA
Last verified: December 2010
History: No changes posted
  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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party: L.E. Pillunat, University of Dresden
ClinicalTrials.gov Identifier: NCT01251705     History of Changes
Other Study ID Numbers: CompCornea
Study First Received: December 1, 2010
Last Updated: December 1, 2010
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

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

ClinicalTrials.gov processed this record on August 25, 2014