Validation of the GATE Software

NCT01265628 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2012-01-26

No results posted yet for this study

Summary

Comparison of the differential luminance sensitivity (DLS) values at each test point

Conditions

  • Visual Field Defects

Interventions

PROCEDURE

perimetry

automated static perimetry with adapted GATE strategy

Sponsors & Collaborators

  • Haag-Streit AG

    collaborator INDUSTRY
  • University Hospital Tuebingen

    lead OTHER

Principal Investigators

  • Ulrich Schiefer, Prof.Dr.med. · University of Tuebingen, Centre for Ophthalmology

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2011-08-31

Countries

  • Germany

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01265628 on ClinicalTrials.gov