Comparation of Different Devices to Measure Corneal Thickness

Corneal Thickness Clinical Trial

Official title:

Comparation of Different Devices to Measure Corneal Thickness

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01251705
• Other study ID #: CompCornea
• Status: Recruiting
• Phase: N/A
• First received: December 1, 2010
• Last updated: December 1, 2010
• Start date: November 2010
• Est. completion date: February 2011

Study information

• Verified date: December 2010
• Source: Technische Universität Dresden
• Contact: Haustein, Doctor med.
• Phone: 0049351458
• Email: Michael.Haustein[@]uniklinikum-dresden.de
• Is FDA regulated: No
• Health authority: Germany: Federal Institute for Drugs and Medical Devices
• Study type: Observational

Clinical Trial Summary

Comparison of different methods for measuring peoples corneal thickness

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 70
• Est. completion date: February 2011
• Est. primary completion date: December 2010
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• healthy cornea

Exclusion Criteria:

• myopia or astigmatism over 1,5 dpt

• corneal surgery

• acute ocular inflammation

• lost of vision

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Corneal Thickness

Locations

Country	Name	City	State
Germany	Departement of Ophthalmology	Dresden	Saxonia

Sponsors (1)

Lead Sponsor	Collaborator
Technische Universität Dresden

Country where clinical trial is conducted

Germany,